{"title":"Chemicals by Class › Compounds by Functional Group › Boron Compounds","description":"\u003cp\u003eSenyawa boron dari TCI untuk reaksi Suzuki-Miyaura: asam boronat aromatik, heteroaromatik, alifatik, boronate ester pinakol, dan potassium trifluoroborate. Distributor resmi TCI di Indonesia: AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510c292617824","title":"TCI C2926 419536-33-7 4-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used as a building block in the synthesis of complex organic molecules. This compound features a heterocyclic structure, combining a carbazole ring with a phenyl ring connected via a boronic acid group. Its unique molecular structure makes it a valuable resource for chemists working on the development of new compounds with specific biological activities. In laboratory settings, it plays a crucial role in synthetic chemistry, particularly in the creation of advanced pharmaceutical and material science applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its stability and reactivity in various chemical reactions, especially those involving boron-based coupling reactions such as the Suzuki and Negishi reactions. These reactions are essential in the synthesis of complex organic structures, making this compound a preferred choice for researchers aiming to create functional molecules. Its ability to form stable bonds with different ligands enhances its versatility in synthetic applications, allowing for the design of compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the fields of pharmaceutical development and advanced material synthesis. Its structural complexity and chemical versatility make it an essential tool for scientists working on innovative projects. Due to its high reactivity and adaptability, it is a key component in the pursuit of new compounds with specific biological or functional properties.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the development of pharmaceutical compounds due to its reactivity in boron-based coupling reactions.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials through the formation of complex molecular structures with high functional specificity.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the design of bioactive molecules with targeted biological effects.\u003c\/li\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds, leveraging its unique carbazole and phenyl ring structure.\u003c\/li\u003e\n\u003cli\u003eUse in academic and industrial research settings for the exploration of new chemical functionalities and applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 419536-33-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its reactivity. Due to its potential reactivity, it should be handled in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper disposal procedures are followed in accordance with local regulations. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086203334874,"sku":"TCI2510C292617824","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086203367642,"sku":"TCI2510C292617825","price":4645000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2926.jpg?v=1767098992"},{"product_id":"tci2510c296717874","title":"TCI C2967 864377-33-3 3-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. This compound plays a crucial role in the development of complex molecular structures, particularly in the field of heterocyclic chemistry. Its unique structure, combining a carbazole unit with a phenylboronic acid group, makes it a valuable building block for researchers aiming to create new compounds with specific functional properties. Due to its reactivity and compatibility with various functional groups, it is a key component in many synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its ability to participate in boronic acid-based reactions, such as Suzuki and Heck couplings, which are essential in the synthesis of pharmaceuticals and advanced materials. Its chemical stability under controlled conditions allows for reliable handling and storage, making it a dependable reagent in both academic and industrial research. Additionally, its capacity to form stable intermediates enhances its utility in multi-step synthesis processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and drug development. It is a fundamental reagent for scientists working on molecular modifications and structural innovations. Its application spans across various research institutions and universities, supporting advancements in both academic and applied chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive boronic acid group and carbazole core.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drugs requiring complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eMolecular modification studies where precise functional group manipulation is essential.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions such as Suzuki and Heck, which benefit from its stability and reactivity.\u003c\/li\u003e\n\u003cli\u003eAdvanced material synthesis for creating compounds with specific physical and chemical properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 864377-33-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which could affect its reactivity. Due to its potential for interaction with other substances, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment when handling. While no specific hazards are indicated, general laboratory safety practices should be followed to ensure safe usage and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086205268186,"sku":"TCI2510C296717874","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086205300954,"sku":"TCI2510C296717875","price":4165000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2967.jpg?v=1767099042"},{"product_id":"tci2510c335218389","title":"TCI C3352 1189047-28-6 2-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used in laboratory settings for its role in organometallic reactions and the synthesis of complex molecular structures. This reagent is particularly valued for its ability to participate in various chemical transformations, especially in catalytic processes that require precise control over reaction conditions. Its unique structure, combining a boronic acid group with a carbazole ring, makes it a versatile tool for chemists working on advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity and specificity are enhanced by its molecular composition, which allows it to interact effectively in a range of chemical environments. Its stability under certain conditions, combined with its sensitivity to moisture and oxidation, requires careful handling to maintain its effectiveness. The presence of varying amounts of anhydride further influences its reactivity, making it a material that demands attention to storage and application protocols. These characteristics make it a reliable choice for researchers aiming to achieve high precision in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of new compounds and molecular modifications. Its availability and consistent quality make it a preferred option for both academic and industrial research institutions. The compound is particularly useful in applications that require controlled chemical reactions, such as the Suzuki reaction, which is crucial in the synthesis of aromatic and heterocyclic compounds.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki Reaction for the synthesis of aromatic and heterocyclic compounds due to its reactivity and compatibility with palladium catalysts.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring precise control over reaction conditions and functional group transformations.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds through targeted molecular modifications and structural alterations.\u003c\/li\u003e\n\u003cli\u003eResearch in catalytic processes where boronic acid derivatives play a key role in cross-coupling reactions.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical stability and reactivity under varying environmental conditions for academic and industrial studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1189047-28-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 25g, 100g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Keep in a dry, cool place away from moisture and oxidizing agents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to prevent moisture-induced degradation and oxidation. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its chemical integrity. Due to its sensitivity to humidity, it should be handled in a controlled laboratory setting with appropriate ventilation. Avoid exposure to light and heat to preserve its reactivity. Always use appropriate personal protective equipment when handling this material to ensure safety during experiments. Proper storage and handling are essential to maintain its effectiveness in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086236856538,"sku":"TCI2510C335218389","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3352.jpg?v=1768204762"},{"product_id":"tci2510c335318390","title":"TCI C3353 858131-73-4 [4'-(Carbazol-9-yl)-4-biphenylyl]boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[4'-(Carbazol-9-yl)-4-biphenylyl]boronic Acid is a specialized organoboron compound used in organic chemistry laboratories. This reagent plays a critical role in various synthetic processes, particularly in the development of complex molecules with high reactivity. Its unique chemical structure allows it to participate in important reactions such as the Suzuki and Kumada couplings, which are essential for the synthesis of heteroaromatic compounds and polymers. Due to its versatility and effectiveness, it is a valuable tool for researchers working on advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its high reactivity and ability to form stable complexes with transition metals. These properties make it an ideal candidate for catalytic processes and functional group transformations. Its stability under certain conditions also ensures that it can be stored and used reliably over time, which is crucial for maintaining experimental consistency. Additionally, its purity and reactivity make it a trusted choice for precise and reproducible chemical experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in academic and industrial settings. It supports the development of new materials, pharmaceuticals, and advanced chemical products. Its application is especially relevant in institutions focused on chemical synthesis and innovation, where high-quality reagents are essential for reliable results.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions, especially those involving Suzuki and Kumada couplings, due to its reactivity and compatibility with transition metals.\u003c\/li\u003e\n\u003cli\u003eDevelopment of heteroaromatic compounds and polymers, as it facilitates the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in chemical reactions, where its ability to form stable metal complexes enhances reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical and material sciences, where precise chemical transformations are required for compound development.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis projects in academic and industrial laboratories, where high purity and reactivity are essential for experimental success.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 858131-73-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in powder or crystalline form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it away from incompatible substances to avoid any potential chemical reactions. In a laboratory setting, proper ventilation and adherence to standard safety protocols are essential when working with this compound to ensure safe and effective use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086236954842,"sku":"TCI2510C335318390","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086236987610,"sku":"TCI2510C335318391","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3353.jpg?v=1768204763"},{"product_id":"tci2510d405724534","title":"TCI D4057 108847-20-7 Dibenzothiophene-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4057 Dibenzothiophene-4-boronic Acid (CAS 108847-20-7) is an organoboron reagent that carries a boronic acid group at the 4-position of the dibenzothiophene framework. As is common for aromatic boronic acids, this product contains varying amounts of the boroxine anhydride formed by natural intermolecular dehydration. In synthetic laboratories, the compound serves as the nucleophilic partner in Suzuki-Miyaura cross-coupling reactions, the most reliable method for forming carbon-carbon bonds between two aromatic fragments. With this reagent, a dibenzothiophene unit can be attached directly and efficiently onto a target molecular scaffold.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent widely chosen is the character of the dibenzothiophene unit itself. Its rigid, electron-rich tricyclic framework provides high thermal stability, a large triplet energy, and good hole-transporting behaviour, which is why it has become a favoured motif in the design of organic light-emitting diode materials. The 4-position, located adjacent to the sulfur atom, gives a distinctive substitution geometry that influences molecular shape and solid-state packing. It should be noted that the presence of the anhydride causes the effective molecular weight to vary, so stoichiometric calculations should account for this.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, functional materials, and optoelectronics, as well as in industrial R\u0026amp;D units developing new molecular scaffolds. It is normally handled in gram or sub-gram quantities on the bench, weighed out for coupling reactions under inert atmosphere, and stored alongside other moisture-sensitive organometallic reagents in a controlled chemical store.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura cross-coupling: acts as the nucleophilic boron partner that transfers the dibenzothiophene fragment to an aryl halide, forming a robust biaryl carbon-carbon bond under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eOLED material synthesis: introduces a dibenzothiophene unit whose high triplet energy and thermal stability make it a preferred building block for host and charge-transport materials.\u003c\/li\u003e\n\u003cli\u003eHole-transport layer development: the electron-rich tricyclic core imparts good hole-transporting character, so the reagent is useful when constructing molecules intended for hole-transporting functions.\u003c\/li\u003e\n\u003cli\u003eFunctional aromatic scaffold construction: allows direct, efficient attachment of a rigid sulfur-containing tricycle onto larger conjugated frameworks without multi-step protection or functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eStructure-property studies: substitution at the 4-position adjacent to sulfur gives distinctive geometry, letting researchers examine how substitution pattern affects molecular shape and solid-state packing.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 108847-20-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the corresponding boroxine anhydride\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed in a cool, dry place, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, well-ventilated chemical store, away from moisture and sources of ignition. Aromatic boronic acids absorb water and undergo further dehydration to the boroxine on standing, so the container should be closed promptly after each use and, where practicable, kept under an inert atmosphere. Weigh the solid in a fume hood using clean, dry spatulas and glassware. Wear a laboratory coat, safety glasses, and chemically resistant gloves. Because the anhydride content varies, verify stoichiometry before use and consult the manufacturer's safety data sheet for full handling guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086653501658,"sku":"TCI2510D405724534","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086653534426,"sku":"TCI2510D405724535","price":4771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4057.jpg?v=1769141943"},{"product_id":"tci2510d437324951","title":"TCI D4373 668983-97-9 Dibenzothiophene-2-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzothiophene-2-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and coupling reactions. As an organoboron reagent, it plays a crucial role in modern synthetic chemistry, enabling the formation of complex molecular structures. This compound is commonly found in chemical and pharmaceutical laboratories due to its ability to react with various functional groups, such as halides, amines, and hydroxyls. Its versatility makes it an essential tool for researchers working on advanced organic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits stable chemical properties under specific conditions, although it can react with acidic or basic substances. The presence of varying amounts of anhydride in the compound influences its reactivity, necessitating careful handling. It dissolves well in organic solvents such as ethyl acetate and ethanol, which facilitates its use in laboratory processes. These characteristics make it a preferred choice for applications requiring controlled reactivity and solubility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzothiophene-2-boronic Acid is frequently used in organic chemistry research, especially in the development of pharmaceutical compounds and industrial chemicals. Its availability and effectiveness have made it a valuable reagent for both academic and industrial research. Due to its specialized nature, it is often sought after for advanced synthetic projects in the chemical sector.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in Suzuki-Miyaura coupling reactions due to its reactivity with aryl halides, enabling efficient cross-coupling in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eApplied in Kumada-Corriu reactions for the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eEmployed in the synthesis of heterocyclic compounds, where its ability to react with functional groups is essential for structural modifications.\u003c\/li\u003e\n\u003cli\u003eUtilized in pharmaceutical research for the development of new drug compounds, as it contributes to the formation of key molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eIntegrated into industrial chemical processes for the production of specialty chemicals, where controlled reactivity and solubility are critical.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 668983-97-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the batch and supplier\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDibenzothiophene-2-boronic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential to react with acidic or basic substances, it should be handled with care, using appropriate personal protective equipment such as gloves and goggles. It is best stored in a well-ventilated laboratory area to minimize any risk of inhalation. Avoid contact with incompatible materials to ensure safe handling and long-term stability. Proper storage conditions help preserve the compound’s effectiveness for use in various laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086689218778,"sku":"TCI2510D437324951","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086689251546,"sku":"TCI2510D437324952","price":2297000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510d456725193","title":"TCI D4567 100124-06-9 Dibenzofuran-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzofuran-4-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and boron-containing substances. This reagent plays a crucial role in laboratory settings, especially in the development of complex molecular structures. It is commonly employed in coupling reactions such as the Suzuki-Miyaura reaction, which is essential for constructing diverse organic molecules. Its versatility makes it an important tool for researchers in various fields, including pharmacology, materials science, and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under specific conditions and its ability to react with transition metals and electrophilic compounds. These properties make it a preferred choice in reactions requiring boron-based reagents. Its solid form and compatibility with a wide range of reagents enhance its utility in synthetic processes. The compound’s ability to participate in complex chemical reactions further solidifies its importance in modern laboratory practices.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzofuran-4-boronic Acid is extensively used in organic chemistry research, particularly in academic institutions and research organizations. Its broad applications and reliability in chemical reactions make it a valuable resource for scientists working on advanced synthetic methodologies. The compound supports the development of new materials and pharmaceutical compounds, contributing significantly to scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis, particularly in the creation of heterocyclic compounds and boron-containing molecules due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research, where it is used to develop new drug compounds through complex synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eMaterials science applications, as it contributes to the synthesis of advanced materials with unique properties.\u003c\/li\u003e\n\u003cli\u003eAcademic teaching and research in chemistry, providing students and researchers with a reliable reagent for experimental work.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes that require precise and stable boronic acid derivatives for intermediate production.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 100124-06-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 100 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDibenzofuran-4-boronic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its potential reactivity with certain substances, it should be handled in a well-ventilated laboratory setting. Avoid contact with transition metals and electrophilic reagents during storage and use. The compound is best stored in airtight containers made of glass or inert polymer materials to ensure long-term preservation. Always follow standard laboratory safety protocols when handling this reagent to minimize risks associated with chemical exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086697509082,"sku":"TCI2510D456725193","price":633000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086697541850,"sku":"TCI2510D456725194","price":2121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4567.jpg?v=1768205059"},{"product_id":"tci2510d471125390","title":"TCI D4711 227305-69-3 2,3-Dihydrobenzofuran-5-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,3-Dihydrobenzofuran-5-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and boron-containing molecules. This compound plays a crucial role in laboratory settings due to its unique reactivity and structural complexity. The presence of a boron atom makes it a versatile reagent for various chemical transformations, especially in coupling reactions. Its ability to form stable intermediates under controlled conditions makes it an essential tool for chemists working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred for its high reactivity towards organic halides and transition metals, which facilitates the formation of new chemical bonds. Its stability under controlled laboratory conditions ensures consistent performance in synthetic processes. The compound's ability to participate in a wide range of reactions, including Suzuki and Stille couplings, makes it a valuable asset in modern organic synthesis. Its versatility and reliability make it a popular choice among researchers in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,3-Dihydrobenzofuran-5-boronic Acid is commonly used in organic chemistry research, especially in projects involving the synthesis of heterocyclic compounds and boron-based molecules. It is frequently employed in the development of new pharmaceuticals and materials due to its reactivity and compatibility with various synthetic methodologies. Its application in these contexts highlights its importance in advancing chemical research and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions such as Suzuki and Stille for forming carbon-carbon bonds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of boron-containing compounds for pharmaceutical and material science applications.\u003c\/li\u003e\n\u003cli\u003eResearch in transition metal catalysis where boronic acid derivatives are essential.\u003c\/li\u003e\n\u003cli\u003eSynthesis of aromatic and phenolic derivatives through functional group transformations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 227305-69-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize inhalation risks. It should not be stored near incompatible substances such as strong oxidizers or acids. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086704685274,"sku":"TCI2510D471125390","price":1844000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4711.jpg?v=1769180671"},{"product_id":"tci2510d477925480","title":"TCI D4779 1133058-06-6 6,9-Diphenyl-9H-carbazole-3-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6,9-Diphenyl-9H-carbazole-3-boronic Acid is a versatile organic compound widely used in scientific research, particularly in the fields of materials science and semiconductor technology. This compound plays a crucial role in the development of advanced materials due to its unique chemical structure, which allows for flexible chemical modifications. Its ability to form stable bonds with various functional groups makes it an essential building block for creating new materials with tailored properties. In the laboratory, it serves as a key reagent in the synthesis of complex compounds that find applications in optoelectronics and display technologies.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability and controlled reactivity make it a preferred choice for researchers aiming to develop materials with specific optical and electronic characteristics. Its boronic acid functionality enables the formation of covalent bonds with other molecules, which is vital for designing materials with enhanced performance. Additionally, its compatibility with a wide range of synthetic methods allows for greater flexibility in material design. These properties make it a reliable and efficient component in the synthesis of advanced semiconductor materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in semiconductor research, especially in the development of optoelectronic devices such as LEDs and OLEDs. Its role in material innovation aligns with the growing demand for high-performance electronic components. Researchers in Indonesia rely on this compound to explore new applications in display technologies and electronic materials, contributing to the advancement of scientific research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis for optoelectronic devices due to its ability to form stable chemical bonds with functional groups.\u003c\/li\u003e\n\u003cli\u003eDevelopment of advanced display technologies such as OLEDs and LEDs through its role in creating materials with tailored optical properties.\u003c\/li\u003e\n\u003cli\u003eResearch in organic electronics where its chemical versatility supports the design of new electronic materials with specific performance characteristics.\u003c\/li\u003e\n\u003cli\u003eMaterial modification studies that require flexible chemical structures for the creation of novel semiconductor compounds.\u003c\/li\u003e\n\u003cli\u003eInvestigation of boronic acid functionalities in the development of hybrid organic-inorganic materials for electronic applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1133058-06-6\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Varies as per supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (exact form may vary)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. Due to its potential reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it should be stored separately from strong acids and bases to avoid unwanted chemical interactions. Proper ventilation is also essential when working with this compound to ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086708125914,"sku":"TCI2510D477925480","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086708158682,"sku":"TCI2510D477925481","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4779.jpg?v=1769180675"},{"product_id":"tci2510d486925607","title":"TCI D4869 402936-15-6 Dibenzo[b,d]furan-2-ylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4869 Dibenzo[b,d]furan-2-ylboronic Acid is an organoboron reagent that carries a boronic acid group at the 2-position of the dibenzofuran framework. The material acts as the nucleophilic partner in palladium-catalyzed cross-coupling reactions, particularly Suzuki–Miyaura couplings, allowing researchers to attach a dibenzofuran unit in a directed manner onto other aromatic or heteroaromatic cores. In organic synthesis laboratories and materials research, a reagent of this type serves as the link between simple small molecules and larger conjugated architectures, without the researcher having to construct the dibenzofuran ring from scratch through a long and material-intensive sequence of steps.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this reagent a preferred choice are the combination of a rigid, planar, electron-rich dibenzofuran framework with the readily controlled reactivity of the boronic acid group. In line with the product name, the material contains varying amounts of anhydride (boroxine), the condensation form commonly encountered with arylboronic acids. This condition generally does not hinder the progress of the coupling, because the boroxine hydrolyzes back to the boronic acid in aqueous-basic reaction media; nevertheless, researchers need to take it into account when weighing out material and calculating stoichiometry for a given reaction.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this class are typically used in university and institutional research groups working on organic synthesis, medicinal chemistry intermediates, and functional organic materials. They are handled at the bench in small-scale coupling reactions under inert conditions, alongside a palladium catalyst, a base, and a suitable solvent system. Because the dibenzofuran unit is otherwise laborious to build in-house, purchasing the ready-made boronic acid shortens the route considerably for research teams working with limited synthetic infrastructure and time.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the boronic acid group transfers the dibenzofuran unit to aryl or heteroaryl halides under palladium catalysis, making this the reagent's primary and most direct application.\u003c\/li\u003e\n\u003cli\u003eConstruction of conjugated organic materials: the rigid, planar, electron-rich dibenzofuran core is well suited to building extended conjugated architectures for functional materials research programs.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block: researchers can install a dibenzofuran fragment onto candidate scaffolds in a directed way, expanding structural diversity without redesigning the entire synthetic route.\u003c\/li\u003e\n\u003cli\u003eHeteroaromatic scaffold elaboration: the reagent couples to heteroaromatic cores as well as simple arenes, giving synthetic chemists a single partner for a broad range of acceptor substrates.\u003c\/li\u003e\n\u003cli\u003eRoute shortening in multistep synthesis: using this ready-made reagent avoids constructing the dibenzofuran ring in-house through a long, material-intensive sequence, saving both bench time and starting material.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 402936-15-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of anhydride (boroxine), the usual condensation form of arylboronic acids\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale packaging offered by the manufacturer; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original, tightly closed container in a cool, dry place away from moisture, direct sunlight, and sources of ignition, following the conditions stated on the manufacturer's label and safety data sheet. Arylboronic acids are sensitive to humidity, so the container should be closed promptly after weighing and, where practical, handled under an inert atmosphere. Because the material contains varying amounts of boroxine anhydride, take this into account when calculating stoichiometry. Handle in a fume hood using gloves, safety glasses, and a laboratory coat, and keep the container clearly labeled and segregated from incompatible materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086728278234,"sku":"TCI2510D486925607","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086728311002,"sku":"TCI2510D486925608","price":6487000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4869.jpg?v=1768197290"},{"product_id":"tci2510d567926649","title":"TCI D5679 1211417-77-4 (1,3-Dimethyl-1H-imidazol-3-ium-2-yl)trihydroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1,3-Dimethyl-1H-imidazol-3-ium-2-yl)trihydroborate is a chemical compound widely used in catalytic reactions and organic synthesis within laboratory settings. This material plays a crucial role in facilitating chemical transformations by acting as a ligand or catalyst in various processes. Its unique structure allows for strong interactions with transition metals, making it a valuable component in both homogeneous and heterogeneous catalysis. Due to its reactivity and stability under controlled conditions, it is frequently employed in research aimed at improving reaction efficiency and selectivity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, particularly the presence of boron in its structure, contribute to its reactivity and versatility. This makes it an ideal choice for applications requiring high reactivity and metal-binding capabilities. Its stability in specific conditions ensures consistent performance in laboratory experiments, while its sensitivity to moisture and air necessitates careful handling. These characteristics make it a preferred option for researchers seeking reliable and effective catalytic agents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (1,3-Dimethyl-1H-imidazol-3-ium-2-yl)trihydroborate is commonly used in organic chemistry and catalysis research. It is a key material for studies involving hydroformylation, oxidation, and the synthesis of heterocyclic compounds. Many research institutions and universities in Indonesia rely on this compound for experiments that demand high reactivity and selectivity in catalytic processes. Its application is central to advancing chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound due to its ability to act as a ligand and enhance catalytic efficiency in complex chemical transformations.\u003c\/li\u003e\n\u003cli\u003eCatalytic hydrogenation processes utilize this material because of its strong interaction with transition metals, which improves reaction rates and selectivity.\u003c\/li\u003e\n\u003cli\u003eOxidation reactions are supported by this compound’s reactivity, allowing for more controlled and efficient oxidation pathways in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eHydroformylation reactions are enhanced by its metal-binding properties, making it a preferred catalyst for producing aldehydes from alkenes and carbon monoxide.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound synthesis relies on this material’s unique structure, enabling the formation of complex ring systems with high yield and purity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1211417-77-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Carbon-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a dry, cool, and well-ventilated area away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool, and well-ventilated area to prevent moisture absorption and degradation. It is recommended to use airtight containers to minimize exposure to air, which can affect its stability. Due to its sensitivity to environmental factors, it should be handled in a controlled laboratory setting with appropriate personal protective equipment. Avoid direct contact with skin and inhalation of vapors. Ensure that storage conditions are consistent to maintain the compound’s effectiveness in catalytic applications. Always follow standard laboratory safety protocols when working with this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086774743258,"sku":"TCI2510D567926649","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5679.jpg?v=1767109071"},{"product_id":"tci2510d575826743","title":"TCI D5758 162607-19-4 Dibenzofuran-1-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzofuran-1-boronic Acid, supplied by TCI under catalogue number D5758, is an organoboron reagent that combines a dibenzofuran framework with a boronic acid group at the 1-position. In organic synthesis laboratories, this compound serves as the nucleophilic partner in palladium-catalysed cross-coupling reactions, particularly the Suzuki–Miyaura reaction, allowing researchers to attach the dibenzofuran unit directly to another aromatic or heteroaromatic core. Its role matters to teams building conjugated molecules, ligands, and active compound candidates, because a single coupling step can replace a far longer and more complicated synthetic sequence.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this reagent a frequent choice are the controlled reactivity of the boronic acid group together with the stability of the dibenzofuran framework under common coupling conditions. It should be noted that this product contains varying amounts of anhydride (boroxine), the natural condensation form of boronic acids. This condition is normal for reagents of this type and does not prevent its use, but it does mean that stoichiometric calculations are best performed with a slight excess of reagent and verified against the data for the specific lot supplied.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, the reagent is typically used in university research groups and industrial R\u0026amp;D units carrying out methodology development and target-oriented synthesis on a milligram to gram scale. It is normally handled alongside a palladium catalyst, a base, and a degassed solvent system on a Schlenk line or in a standard reflux setup. Because it is an imported specialty reagent, working groups generally plan their coupling experiments around the pack size on hand and record lot information for reproducibility.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the boronic acid group transfers the dibenzofuran unit to aryl or heteroaryl halides under palladium catalysis, making it the reagent's primary and most direct application.\u003c\/li\u003e\n\u003cli\u003eConstruction of conjugated molecules: the rigid, planar dibenzofuran framework is introduced in one step, which suits research groups assembling extended conjugated systems for materials-oriented studies.\u003c\/li\u003e\n\u003cli\u003eLigand synthesis: the dibenzofuran core can be coupled onto aromatic scaffolds to build ligand structures, with the boronic acid providing a predictable and controllable point of attachment.\u003c\/li\u003e\n\u003cli\u003ePreparation of active compound candidates: medicinal chemistry work uses this coupling partner to install the dibenzofuran motif into candidate structures without a long multi-step preparative sequence.\u003c\/li\u003e\n\u003cli\u003eSynthetic methodology development: the reagent's controlled reactivity and framework stability make it a suitable substrate when screening catalysts, bases, and solvent systems for coupling optimisation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D5758\u003c\/li\u003e\n\u003cli\u003eCAS number: 162607-19-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the anhydride (boroxine) condensation form\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research pack sizes offered for this catalogue item; please confirm the current option when ordering\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry place, protected from moisture and away from direct sunlight. Boronic acids are sensitive to humidity, so the container should be closed promptly after each use and allowed to reach room temperature before opening to avoid condensation on the solid. Weighing and transfer are best carried out in a fume hood using clean, dry spatulas and glassware. Wear safety glasses, gloves, and a laboratory coat when handling the material, keep it separate from strong oxidising agents, and dispose of residues and contaminated consumables through the laboratory's chemical waste procedure. Always consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086777888986,"sku":"TCI2510D575826743","price":2576000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086777921754,"sku":"TCI2510D575826744","price":8935000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5758.jpg?v=1769142136"},{"product_id":"tci2510d603227049","title":"TCI D6032 108847-24-1 Dibenzo[b,d]thiophen-3-ylboronic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzo[b,d]thiophen-3-ylboronic Acid is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex heterocyclic compounds. This versatile reagent plays a crucial role in organic chemistry, particularly in the development of molecules with specific biological functions. Its unique structure, featuring boron and sulfur atoms, contributes to its reactivity and stability, making it an essential component in various chemical reactions. Researchers rely on this compound to create new substances with tailored chemical and biological properties, supporting advancements in pharmaceutical and material sciences.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and functional group make it a preferred choice for synthetic chemists. Its ability to participate in coupling reactions, substitution processes, and interactions with diverse reagents enhances its utility in laboratory applications. The presence of boronic acid functionality allows for efficient cross-coupling reactions, which are fundamental in the synthesis of complex organic molecules. These properties make it a valuable tool for scientists aiming to design and develop novel compounds with specific functionalities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzo[b,d]thiophen-3-ylboronic Acid is commonly used in research related to organic chemistry, pharmacology, and materials science. It is particularly favored in academic and industrial settings where the synthesis of bioactive compounds and advanced materials is required. Its role in drug discovery and the development of new chemical materials underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive boronic acid group and sulfur-containing structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules in pharmacological research for drug discovery and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials in material science through cross-coupling reactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eSupport for synthetic pathways in academic and industrial laboratories requiring complex molecule construction.\u003c\/li\u003e\n\u003cli\u003eUse in chemical research for studying reactivity and stability of functional groups in various reaction conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 108847-24-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDibenzo[b,d]thiophen-3-ylboronic Acid should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect the compound from moisture and air exposure. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound is best stored in a well-ventilated area to minimize any potential risks associated with its chemical properties. Proper labeling and storage conditions are essential to ensure safe handling and long-term stability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086788604122,"sku":"TCI2510D603227049","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086788636890,"sku":"TCI2510D603227050","price":3636000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6032.jpg?v=1767109607"},{"product_id":"tci2510e115329063","title":"TCI E1153 669072-93-9 9-Ethylcarbazole-3-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-Ethylcarbazole-3-boronic Acid is an organoboron compound widely utilized in chemical laboratories for its unique reactivity and versatility in synthetic applications. This compound plays a crucial role in organic synthesis, particularly in coupling reactions that enable the formation of complex molecular structures. Its presence in various chemical processes makes it an essential reagent for researchers working on advanced chemical transformations. Due to its structural characteristics, it is often employed in reactions involving boronic acids and their derivatives, offering a reliable and efficient pathway for compound development.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity stems from its boronic acid functionality, which allows it to participate in a range of chemical interactions. Its ability to form stable bonds with various ligands enhances its utility in synthetic chemistry. Additionally, its chemical stability under controlled conditions makes it a preferred choice for laboratory applications. However, it is sensitive to moisture and oxidation, which necessitates careful handling and storage. These properties make it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-Ethylcarbazole-3-boronic Acid is commonly used in chemical and pharmaceutical research. It supports the development of new compounds with potential biological activity, contributing to advancements in drug discovery and synthetic chemistry. Its availability in solid form simplifies handling and measurement, making it a practical choice for routine laboratory use. The compound’s role in organic synthesis is well-established, and its application continues to expand in both research and development contexts.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound’s reactivity and stability, making it ideal for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions, such as Suzuki and Kumada, rely on its ability to form stable bonds with various ligands, enhancing reaction efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes it for the development of new compounds with potential therapeutic applications and biological activity.\u003c\/li\u003e\n\u003cli\u003eIt supports the synthesis of advanced organic molecules, contributing to the creation of novel chemical entities in research laboratories.\u003c\/li\u003e\n\u003cli\u003eIts solid form facilitates accurate measurement and handling, making it suitable for routine chemical experiments and laboratory protocols.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 669072-93-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires protection from moisture and oxidation; store in a cool, dry place.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to prevent moisture and oxidation exposure. It is recommended to use airtight containers to maintain its chemical integrity and prevent degradation. Due to its potential corrosive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the laboratory. The compound’s sensitivity to environmental factors necessitates careful storage and handling to maintain its effectiveness in chemical applications. Always follow standard laboratory safety protocols when working with this reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086929440986,"sku":"TCI2510E115329063","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086929473754,"sku":"TCI2510E115329064","price":7143000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1153.jpg?v=1768205262"},{"product_id":"tci2510f054830434","title":"TCI F0548 1369328-62-0 5'-Formyl-2,2'-bithiophene-5-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5'-Formyl-2,2'-bithiophene-5-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and complex molecules. This reagent contains both a boronic acid group and a formyl group, which contribute to its reactivity and specificity in various chemical transformations. Its unique molecular structure makes it a valuable tool in synthetic chemistry, especially in the development of advanced materials and electronic components. Due to its complex structure and the presence of anhydride, this compound exhibits high reactivity and can participate in a wide range of chemical interactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity is enhanced by its ability to form stable intermediates during coupling and substitution reactions. Its chemical versatility allows it to be used in multiple synthetic pathways, making it a preferred choice for researchers working on complex molecule synthesis. The presence of the boronic acid group also facilitates its use in cross-coupling reactions, which are essential in the creation of functionalized organic compounds. These properties make it a key reagent in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of materials with applications in electronics and advanced chemical synthesis. It is also integral to studies involving the synthesis of heterocyclic compounds and complex molecular structures. Its role in scientific innovation is significant, supporting the development of new materials and chemical processes in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and functional groups.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex molecular structures in material science research.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reactions for functionalization of organic molecules.\u003c\/li\u003e\n\u003cli\u003eSynthesis of electronic materials for advanced applications in semiconductor technology.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical engineering for the creation of new polymers and nanomaterials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1369328-62-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its chemical properties. Due to its reactive nature, it should be handled in a well-ventilated laboratory setting, with appropriate personal protective equipment such as gloves and safety goggles. It is important to avoid contact with incompatible substances and to follow standard chemical safety protocols to ensure safe handling and storage. Proper labeling and storage conditions are essential to maintain the integrity of the compound and ensure safe usage in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087012966618,"sku":"TCI2510F054830434","price":9969000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0548.jpg?v=1768205359"},{"product_id":"tci2510f054930435","title":"TCI F0549 4347-33-5 5-Formyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Formyl-2-thiopheneboronic Acid is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. It serves as a crucial building block in the creation of complex molecular structures, particularly in heterocyclic chemistry. This compound is commonly found in chemical laboratories, where it acts as a key reagent in various synthetic pathways. Its unique combination of a thiophene ring and a boronic acid group makes it a valuable tool for chemists working on the development of new compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and compatibility with a range of chemical reactions make it a preferred choice for researchers. It is particularly effective in coupling reactions, substitution reactions, and boron-based chemical transformations. These properties enable it to be a reliable component in the synthesis of pharmaceuticals, materials, and other advanced chemical products. Its ability to participate in multiple reaction types enhances its utility in diverse research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Formyl-2-thiopheneboronic Acid is frequently used in organic chemistry research, especially in fields such as pharmacology and material science. It is a staple in academic and industrial research settings, where its chemical properties support the development of new compounds and materials. Its stability under controlled conditions also makes it a practical choice for routine laboratory use.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where this compound is used to build complex molecular structures due to its reactivity and compatibility with various reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its use in the development of new drugs, as it can contribute to the synthesis of bioactive compounds with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications rely on its ability to participate in boron-based reactions, enabling the creation of advanced functional materials.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound synthesis is enhanced by its unique thiophene and boronic acid structure, making it ideal for constructing diverse chemical frameworks.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesian universities often incorporates this compound to explore new synthetic methodologies and chemical transformations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4347-33-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air, which may affect its stability. Proper ventilation is essential when handling the material to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. It should be stored away from incompatible substances to ensure safety. Regular monitoring of storage conditions is advised to ensure optimal preservation of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087012999386,"sku":"TCI2510F054930435","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087013032154,"sku":"TCI2510F054930436","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0549.jpg?v=1767113723"},{"product_id":"tci2510f080130772","title":"TCI F0801 17303-83-2 3-Formyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F0801 3-Formyl-2-thiopheneboronic Acid is a dual-functional organoboron reagent designed for the demands of modern organic synthesis, particularly the construction of carbon–carbon bonds. The compound is built around a thiophene core, a five-membered heterocycle encountered very frequently in the molecular frameworks of pharmaceuticals and organic electronic materials. The second position carries a boronic acid group that acts as the nucleophilic partner in cross-coupling reactions, while the third position bears a formyl (aldehyde) group that supplies a second reactive site. This combination makes it a highly valued starting material for synthetic chemistry laboratories, medicinal chemistry programmes, and research into thiophene-based functional materials.\u003c\/p\u003e\n\u003cp\u003eThe most distinctive characteristic of this reagent is its bifunctional nature. Researchers can engage the boronic acid group first through a Suzuki–Miyaura reaction with an aryl halide, then elaborate the still-intact aldehyde group through condensation, reduction, reductive amination, or the construction of further heterocyclic rings. A stepwise approach of this kind shortens synthetic routes and reduces the need for protecting-group manipulations. The material is supplied as containing varying amounts of the corresponding anhydride, which is normal for boronic acids of this class and is accounted for in routine stoichiometric calculations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on synthetic organic chemistry, medicinal chemistry, and organic electronic materials. It suits methodology development, the preparation of thiophene-containing intermediates, and small-scale exploratory syntheses where a compact bifunctional building block saves both time and reagents. Because it is supplied in laboratory-scale packaging from TCI, it fits well into the workflow of research groups that order defined quantities for specific project stages rather than bulk production.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the boronic acid group at position two transfers the thiophene unit to aryl or heteroaryl halides under palladium catalysis, giving biaryl products with the aldehyde preserved for later use.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block: the thiophene core is a recurring motif in drug scaffolds, and two orthogonal reactive handles allow rapid assembly of analogue libraries from a single common intermediate.\u003c\/li\u003e\n\u003cli\u003eOrganic electronic materials research: thiophene-based frameworks underpin many conjugated systems, and this reagent introduces a thiophene unit already carrying an aldehyde for further conjugation or condensation chemistry.\u003c\/li\u003e\n\u003cli\u003eHeterocycle construction: the free formyl group serves as the entry point for cyclisation and condensation sequences that build additional fused or pendant heterocyclic rings onto the coupled product.\u003c\/li\u003e\n\u003cli\u003eAldehyde derivatisation chemistry: after coupling, the intact aldehyde can be carried into reductive amination, reduction to the alcohol, or condensation with amines and active methylene compounds without extra protecting steps.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 17303-83-2\u003c\/li\u003e\n\u003cli\u003eProduct Code: F0801\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the corresponding anhydride\u003c\/li\u003e\n\u003cli\u003ePackaging: supplied in laboratory-scale research pack sizes as listed by the manufacturer\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry place, protected from moisture and away from direct sunlight, following the storage conditions stated on the manufacturer's label and Safety Data Sheet. Boronic acids are best kept in their original tightly sealed containers, and repeated exposure to humid air should be avoided when weighing out portions. Handle the material in a fume hood using safety goggles, gloves, and a laboratory coat, and avoid generating or inhaling dust. Keep it separate from strong oxidising agents, and consult the current Safety Data Sheet before use, transfer, or disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087032725722,"sku":"TCI2510F080130772","price":3408000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087032758490,"sku":"TCI2510F080130773","price":13249000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0801.jpg?v=1768205388"},{"product_id":"tci2510f106531137","title":"TCI F1065 175592-59-3 (5-Formylthiophen-3-yl)boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(5-Formylthiophen-3-yl)boronic Acid is a versatile organic compound widely used in laboratory settings for its role in various synthetic reactions. It serves as a key reagent in the synthesis of heterocyclic compounds and complex molecular structures, making it essential for advanced chemical research. This compound is particularly valuable in the field of organoboron chemistry, where it contributes to the development of new materials and pharmaceutical compounds. Its unique chemical properties allow it to participate in multiple reaction pathways, enhancing its utility across different experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity and ability to form stable bonds with organic ligands and metals. These properties make it a preferred choice for reactions such as the Suzuki-Miyaura and Heck coupling reactions, which are fundamental in organic synthesis. Its stability under certain conditions ensures reliable results, making it a trusted reagent in both academic and industrial laboratories. The combination of reactivity and stability allows researchers to achieve precise and consistent outcomes in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (5-Formylthiophen-3-yl)boronic Acid is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. Its availability and reliability make it a staple in chemical laboratories, supporting a wide range of experimental needs. The compound's role in creating new molecular structures underscores its importance in advancing scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and ability to form stable bonds with various ligands.\u003c\/li\u003e\n\u003cli\u003eUse in Suzuki-Miyaura coupling reactions for efficient cross-coupling of aryl halides with boronic acids.\u003c\/li\u003e\n\u003cli\u003eApplication in Heck reactions for the formation of carbon-carbon bonds in complex molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eSupport in the development of pharmaceutical compounds through its role in creating boron-containing structures.\u003c\/li\u003e\n\u003cli\u003eUtilization in material science research for the synthesis of advanced polymers and functional materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 175592-59-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Varies as per supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which can affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated area to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. Proper disposal methods should be followed to ensure compliance with environmental and safety regulations. The compound is not classified as hazardous under standard laboratory conditions, but standard chemical safety protocols should still be observed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087055499482,"sku":"TCI2510F106531137","price":5831000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087055532250,"sku":"TCI2510F106531138","price":21426000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1065.jpg?v=1769142450"},{"product_id":"tci2510f142131566","title":"TCI F1421 2396648-06-7 Spiro[fluorene-9,9'-xanthen]-2'-ylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSpiro[fluorene-9,9'-xanthen]-2'-ylboronic Acid is a specialized organic compound used in advanced laboratory settings, particularly in the field of organometallic chemistry. This reagent plays a crucial role in facilitating complex organic syntheses, especially in reactions that require the introduction of boronic acid functionalities. Its unique structure allows it to participate in various coupling reactions, making it an essential component in the development of new chemical compounds. Due to its reactivity and versatility, it is widely used in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound’s spiro structure, combined with its boronic acid functionality, contributes to its high reactivity and stability under controlled laboratory conditions. This unique combination of properties makes it a preferred choice for chemists working on synthetic pathways that demand both structural integrity and chemical reactivity. Its ability to form stable intermediates during reactions enhances its utility in multi-step synthesis processes. Additionally, its compatibility with a wide range of ligands and substrates broadens its applicability in diverse chemical transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of complex heterocyclic compounds and pharmaceutical intermediates. It is a key reagent in the development of new drugs and materials, supporting both fundamental research and applied scientific projects. Its presence in Indonesian academic and industrial laboratories underscores its importance in advancing chemical innovation and scientific discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and compatibility with coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical intermediates as it supports the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eResearch in organoboron chemistry for its unique spiro structure and boronic acid functionality.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in Suzuki-Miyaura coupling reactions, where it acts as a key reagent.\u003c\/li\u003e\n\u003cli\u003eInvestigation of new chemical materials in advanced materials science research applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2396648-06-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct light to maintain its chemical integrity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. In laboratory settings, it should be kept in a well-ventilated area to minimize exposure to vapors. Regular monitoring of storage conditions is advised to ensure optimal performance and safety during use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087083417818,"sku":"TCI2510F142131566","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1421.jpg?v=1769142481"},{"product_id":"tci2510i080336069","title":"TCI I0803 147621-18-9 6-Indoleboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Indoleboronic Acid (TCI I0803) is a chemical compound widely used in laboratory settings for its unique reactivity in organometallic reactions. This reagent plays a crucial role in the synthesis of heterocyclic compounds and boron-containing molecules, making it an essential tool for chemists working in synthetic chemistry. Its structural features, including the presence of a boronic acid group, enable it to participate in various chemical transformations such as coupling reactions, reductions, and substitutions. Due to its versatility, it is frequently employed in research aimed at creating complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make 6-Indoleboronic Acid a preferred choice is its ability to form stable complexes with transition metals. This characteristic allows it to be used in the development of organometallic compounds, which are vital in both academic and industrial research. Additionally, its solubility in organic solvents enhances its usability across a wide range of chemical processes. The compound’s reactivity and compatibility with various reagents make it a reliable and efficient material for laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Indoleboronic Acid is extensively used in organic chemistry research, particularly in the fields of pharmacology, material science, and biochemical synthesis. Its relevance lies in its ability to facilitate the formation of complex structures that are essential for drug development and advanced material design. Researchers in Indonesia rely on this compound for its consistent performance and adaptability in different experimental conditions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity in coupling reactions and its ability to form stable boron-containing intermediates.\u003c\/li\u003e\n\u003cli\u003eDevelopment of transition metal complexes for catalytic applications, leveraging its capacity to bind with metal ions and enhance reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eBiochemical synthesis of complex molecules, as it supports the construction of structures involving boron and nitrogen atoms in biologically relevant contexts.\u003c\/li\u003e\n\u003cli\u003eMaterial science research for creating new boron-based materials with unique electronic and structural properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of drug molecules that require boronic acid functionalities for improved biological activity and stability.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 147621-18-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Indoleboronic Acid should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture, which can affect its reactivity. The material should be stored away from incompatible substances such as strong oxidizers to ensure safety in the laboratory. Proper labeling of storage containers is essential for easy identification and safe handling. Regular inspection of storage conditions is advised to ensure optimal preservation of the compound. All handling should be performed with appropriate personal protective equipment to minimize exposure risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087417848026,"sku":"TCI2510I080336069","price":12114000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0803.jpg?v=1768205620"},{"product_id":"tci2510i104036381","title":"TCI I1040 1023595-17-6 Indazole-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIndazole-4-boronic Acid (1023595-17-6) is a chemical compound widely used in organic laboratory settings. It serves as a versatile reagent in various synthetic processes, particularly in the formation of heterocyclic compounds and coupling reactions. This compound is a key component in modern synthetic chemistry due to its ability to participate in multiple reaction pathways. Its structural features, including the presence of a boronic acid group, make it highly reactive under specific conditions, enabling it to form stable intermediates with a variety of substrates. This reactivity is crucial in the development of complex molecules in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique chemical properties make it a preferred choice for chemists working in advanced synthesis. Its boronic acid functionality allows for efficient coupling reactions, such as the Suzuki-Miyaura and Kumada-Corriu reactions, which are essential in the synthesis of pharmaceuticals and materials. Additionally, the presence of anhydride impurities can influence its reactivity, making it important to consider during synthesis planning. These characteristics ensure that it remains a valuable tool in the hands of researchers aiming for controlled and reproducible chemical transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Indazole-4-boronic Acid is commonly used in organic chemistry research, especially in the development of pharmaceutical compounds and inorganic materials. Its ability to react under controlled conditions makes it a go-to reagent for scientists working on complex molecular structures. Researchers in educational and research institutions frequently rely on this compound for its reliability and effectiveness in various synthetic applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and coupling capabilities.\u003c\/li\u003e\n\u003cli\u003eUse in Suzuki-Miyaura cross-coupling reactions for efficient carbon-carbon bond formation.\u003c\/li\u003e\n\u003cli\u003eApplication in Kumada-Corriu coupling for the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical development for the creation of novel drug compounds.\u003c\/li\u003e\n\u003cli\u003eInvestigation of inorganic material synthesis through controlled chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1023595-17-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As listed on product page\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eIndazole-4-boronic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential reactivity with heavy metals and oxidizing agents, it should be handled with care, using appropriate personal protective equipment. Storage away from incompatible substances is essential to ensure safety in the laboratory. Regular monitoring of storage conditions is advised to maintain the integrity of the compound during long-term use. Proper labeling and containment are necessary to prevent accidental exposure and ensure safe handling practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087436230874,"sku":"TCI2510I104036381","price":3787000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1040.jpg?v=1768361088"},{"product_id":"tci2510l036737328","title":"TCI L0367 244761-29-3 Lithium Bis(oxalate)borate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eLithium Bis(oxalate)borate (LiBOB) is a chemical compound widely used in various organometallic reactions and synthetic chemistry processes. As an organoboron reagent, it plays a crucial role in substitution reactions and other boron-involved chemical transformations. This compound is particularly valued for its ability to participate in complex molecule modifications and the synthesis of advanced chemical structures. In laboratory settings, LiBOB is employed to facilitate reactions that require specific stability and reactivity characteristics, making it an essential tool for chemists working on intricate synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eLiBOB is favored for its chemical stability under controlled conditions and its reactivity towards uncontrolled environments. Its complex molecular structure allows it to interact effectively with both organic and inorganic compounds, enhancing its versatility in laboratory applications. The compound’s ability to maintain stability while exhibiting controlled reactivity makes it a preferred choice for researchers aiming to achieve precise chemical outcomes. These properties ensure that LiBOB remains a reliable and effective reagent in a wide range of chemical experiments and syntheses.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, LiBOB is commonly used in organic chemistry research and the synthesis of complex compounds. It is a key component in studies requiring reagents with specific chemical properties to produce desired chemical products. Its application is widespread in both academic and industrial research settings, where its unique characteristics support the development of new chemical materials and processes. The compound’s reliability and effectiveness make it an essential part of the laboratory toolkit in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where precise reactivity and stability are required.\u003c\/li\u003e\n\u003cli\u003eModification of organic molecules to create complex chemical structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003eResearch into boron-based chemical transformations and their mechanisms.\u003c\/li\u003e\n\u003cli\u003ePreparation of specialized reagents for advanced chemical processes in laboratory settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 244761-29-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and incompatible substances.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eLiBOB should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which can affect its reactivity. Proper labeling of storage containers is essential to ensure safe handling. Laboratory personnel should wear appropriate personal protective equipment when handling this compound. It should be stored away from incompatible materials such as strong acids or bases. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in chemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087497113818,"sku":"TCI2510L036737328","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087497146586,"sku":"TCI2510L036737329","price":4821000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0367.jpg?v=1768361236"},{"product_id":"tci2510m185039917","title":"TCI M1850 162607-20-7 5-Methyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M1850 5-Methyl-2-thiopheneboronic Acid is an organoboron reagent that combines a methylated thiophene ring with a boronic acid group at the second position. As is common for aryl and heteroaryl boronic acids, this material may contain varying amounts of the cyclic anhydride known as a boroxine, formed through intermolecular loss of water, and this is openly stated in the product name itself. Its role in the laboratory is clear and well defined: it serves as the nucleophilic partner in the Suzuki–Miyaura cross-coupling reaction, one of the most dependable methods available for joining two aromatic fragments together.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this reagent a preferred choice is the balance it strikes between reactivity and ease of handling. Boronic acids are relatively non-toxic and are stable toward air and water when compared with other organometallic reagents such as organolithium or Grignard compounds, yet they remain reactive enough to transfer the thienyl group to the palladium centre during the transmetalation step. The electron-rich thiophene ring contributes valuable electronic character to conjugated materials, while the methyl group at the fifth position improves solubility in organic solvents and simultaneously blocks that position so that the direction of coupling is more readily controlled.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in synthetic organic chemistry groups at universities and research institutes, as well as in laboratories developing conjugated and functional materials. It is used on the bench scale for building blocks in medicinal chemistry programmes, for preparing thiophene-containing intermediates, and in graduate research projects where Suzuki–Miyaura coupling forms the central step of a synthetic route.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling — the reagent acts as the nucleophilic boron partner that transfers its thienyl group to the palladium centre during transmetalation, making it directly suited to joining aromatic fragments.\u003c\/li\u003e\n\u003cli\u003eSynthesis of conjugated materials — the electron-rich thiophene ring contributes useful electronic character to extended conjugated systems, which is precisely why thiophene boronic acids are selected for these constructions.\u003c\/li\u003e\n\u003cli\u003ePreparation of biaryl and heterobiaryl intermediates — coupling a thiophene unit to another aromatic fragment is a reliable route to mixed aromatic scaffolds required in multi-step synthetic work.\u003c\/li\u003e\n\u003cli\u003eRegiocontrolled coupling work — the methyl group occupying the fifth position closes off that site, so the direction of coupling is more controlled and the outcome of the reaction is more predictable.\u003c\/li\u003e\n\u003cli\u003eBench-scale medicinal chemistry building-block synthesis — the relatively low toxicity and stability toward air and water make it far more practical to handle routinely than organolithium or Grignard alternatives.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 162607-20-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eProduct code: M1850\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the cyclic anhydride (boroxine)\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the packaging options listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage: store in a cool, dry place in a tightly closed container\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a cool, dry location in its original tightly closed container, kept away from moisture, since boronic acids undergo intermolecular loss of water to form the corresponding boroxine anhydride. Containers should be well sealed and clearly labelled, and the material should be returned to storage promptly after weighing. Handle in a fume hood using standard laboratory personal protective equipment, including safety goggles, a laboratory coat, and suitable gloves. Avoid raising dust when transferring the solid, and keep the material separated from incompatible substances. Always consult the manufacturer's Safety Data Sheet before use, and follow your institution's chemical waste procedures for disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087632675034,"sku":"TCI2510M185039917","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087632707802,"sku":"TCI2510M185039918","price":4292000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1850.jpg?v=1769142923"},{"product_id":"tci2510m203540151","title":"TCI M2035 94839-07-3 3,4-(Methylenedioxy)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,4-(Methylenedioxy)phenylboronic Acid is a chemical compound widely used in organic laboratory settings for its versatile reactivity and functional group versatility. This compound belongs to the organoboron reagent family and is particularly valuable in synthetic chemistry due to its ability to participate in various reaction mechanisms. Its unique structure, featuring a methylenedioxy group attached to a phenylboronic acid core, makes it an essential component in the synthesis of complex organic molecules. This reagent is commonly employed in coupling reactions, where it facilitates the formation of new carbon-carbon bonds, making it a key player in modern synthetic strategies.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and compatibility with a wide range of substrates make it a preferred choice for organic chemists. Its ability to undergo hydrolysis and substitution reactions allows for the creation of diverse molecular architectures. Additionally, its stability under controlled laboratory conditions ensures consistent performance, which is crucial for reproducible results. These properties make it a reliable and efficient reagent for both academic and industrial research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in organic synthesis research, particularly in universities and research institutions. Its relevance in the development of new compounds and functional materials makes it a staple in the chemical research toolkit. The compound’s availability and performance make it a go-to reagent for chemists working on complex molecular transformations and functional group manipulations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where this reagent is used to facilitate coupling reactions and the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eFunctional group manipulation benefits from its reactivity, allowing for the modification of aromatic compounds through substitution and hydrolysis.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes often utilize this compound due to its ability to participate in various reaction mechanisms, enhancing reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eMaterial synthesis relies on its reactivity to create new compounds with specific properties, making it essential in polymer and pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications benefit from its stability and reactivity, enabling accurate and reliable experimental outcomes in various testing scenarios.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 94839-07-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its performance. When handling, it is important to use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. The compound should be stored in a well-ventilated area to minimize any potential risks associated with its chemical nature. Proper labeling of containers is essential to ensure safe handling and prevent accidental misuse. Regular inspection of storage conditions is advised to maintain optimal performance and safety standards in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087643488474,"sku":"TCI2510M203540151","price":2197000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087643521242,"sku":"TCI2510M203540152","price":7748000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2035.jpg?v=1768205770"},{"product_id":"tci2510m268041018","title":"TCI M2680 720702-41-0 (1-Methyl-1H-pyrazol-5-yl)boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1-Methyl-1H-pyrazol-5-yl)boronic Acid is a chemical compound widely used in laboratory settings for its role in organometallic reactions. This reagent contains a boronic acid group attached to a pyrazol ring, making it a valuable component in the synthesis of complex organic molecules. Its unique structure allows it to participate in various chemical transformations, particularly in coupling reactions that are essential for building molecular frameworks. This compound is commonly found in synthetic chemistry workflows where the formation of carbon-carbon bonds is required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity and compatibility with transition metals make it a preferred choice for researchers. Its ability to form stable complexes with metals under specific conditions enhances its utility in catalytic processes. The presence of the boronic acid group also contributes to its versatility, enabling it to act as a nucleophile or electrophile depending on the reaction conditions. These properties make it a reliable and effective reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (1-Methyl-1H-pyrazol-5-yl)boronic Acid is frequently used in organic chemistry research. It plays a key role in the development of new compounds and the study of molecular structures. Its application extends to projects focused on the synthesis of bioactive molecules, including pharmaceuticals and industrial chemicals. The compound’s importance in coupling reactions, such as Suzuki and Stille, further solidifies its position as a critical reagent in modern synthetic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki Coupling Reactions: This reagent is ideal for Suzuki coupling due to its compatibility with palladium catalysts and its ability to form stable aryl-boron intermediates.\u003c\/li\u003e\n\u003cli\u003eStille Coupling Applications: It is frequently used in Stille coupling to facilitate the formation of carbon-carbon bonds in complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis of Aromatic Compounds: Its structure enables it to participate in the synthesis of aromatic compounds with high efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of Bioactive Molecules: Researchers use it to create compounds with potential pharmaceutical or industrial applications through targeted synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eStructural Studies of Organic Molecules: It is employed in the investigation of molecular structures due to its reactivity and ability to form diverse chemical bonds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 720702-41-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Varies as per supplier\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture, which can affect its reactivity. Due to its potential reactivity with certain substances, it should be handled in a well-ventilated area and stored away from incompatible materials. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this reagent. Proper storage conditions ensure the material remains stable and effective for use in various synthetic processes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087708401882,"sku":"TCI2510M268041018","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087708434650,"sku":"TCI2510M268041019","price":3887000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2680.jpg?v=1768205819"},{"product_id":"tci2510m284041246","title":"TCI M2840 162607-15-0 4-Methyl-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Methyl-2-thiopheneboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and coupling reactions. This reagent plays a crucial role in laboratory settings where the formation of new chemical bonds is required. Its unique structure, containing both boronic acid and thiophene groups, enhances its reactivity under various chemical conditions. This versatility makes it an essential component in the toolkit of chemists working in diverse research fields.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity is further enhanced by the presence of varying amounts of anhydride, which provides flexibility in its application. This characteristic allows it to participate in a wide range of reactions, including those involving different ligands and metals. Its ability to interact with various organic compounds makes it a preferred choice for researchers aiming to develop new materials, pharmaceuticals, and environmental chemicals. The compound's chemical complexity ensures that it remains a valuable asset in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Methyl-2-thiopheneboronic Acid is commonly used in organic chemistry research, especially in the fields of pharmacy, materials science, and environmental chemistry. Its role in catalytic reactions and synthetic pathways has made it a staple in both academic and industrial research environments. The compound's adaptability and reactivity continue to drive innovation in chemical synthesis and development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this reagent is used for coupling reactions and heterocyclic compound formation due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its ability to participate in complex synthetic pathways, aiding in the development of new drug molecules and therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eMaterials science applications rely on its reactivity to create novel polymers and functional materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental chemistry studies utilize it for the synthesis of compounds used in pollution control and remediation processes.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesia frequently employs this compound to explore new chemical reactions and synthetic methodologies in both undergraduate and postgraduate studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 162607-15-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Avoid contact with incompatible substances to ensure safe usage. Regular monitoring of storage conditions is advised to maintain optimal performance and safety in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087718265050,"sku":"TCI2510M284041246","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087718297818,"sku":"TCI2510M284041247","price":4645000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2840.jpg?v=1769142999"},{"product_id":"tci2510m296741419","title":"TCI M2967 904326-93-8 6-(Morpholino)pyridine-3-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-(Morpholino)pyridine-3-boronic Acid is a chemical compound widely used in organic reactions, especially in the synthesis of heterocyclic compounds and boron-containing molecules. Its complex structure enables high reactivity under various chemical conditions, making it a valuable tool in synthetic chemistry. This compound is commonly employed as a reagent in coupling reactions, such as the Suzuki-Miyaura reaction, which is essential for the synthesis of complex molecules. Its reactivity is particularly notable towards transition metals and other organic compounds, enhancing its utility in diverse chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe presence of varying amounts of anhydride in this compound provides flexibility in chemical reactions, allowing for a range of synthetic pathways. Its unique molecular structure enables the formation of complex bonds, making it a preferred choice for researchers seeking versatile reagents. The compound’s ability to participate in multiple reaction types and its compatibility with various reaction conditions contribute to its popularity in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in organic chemistry research, particularly in higher education institutions and research organizations. Its availability, reliability, and effectiveness in a wide array of chemical reactions make it a top choice for local researchers. The compound plays a crucial role in advancing chemical synthesis and innovation within the scientific community in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura Coupling Reactions: This compound is ideal for coupling reactions due to its reactivity with transition metals and its ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis of Heterocyclic Compounds: Its unique molecular structure allows it to participate in the synthesis of various heterocyclic compounds, enhancing the diversity of chemical products.\u003c\/li\u003e\n\u003cli\u003eBoron-Containing Molecule Synthesis: The compound is well-suited for the creation of boron-based molecules, which are essential in pharmaceutical and materials science research.\u003c\/li\u003e\n\u003cli\u003eTransition Metal Catalyzed Reactions: Its reactivity with transition metals makes it a suitable reagent for catalytic processes in synthetic chemistry.\u003c\/li\u003e\n\u003cli\u003eComplex Bond Formation in Organic Chemistry: Its ability to form new and complex bonds makes it a valuable tool in the development of advanced chemical structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 904326-93-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from moisture and direct light to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its chemical properties. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation should be maintained in the laboratory to minimize inhalation risks. The compound should not be stored near incompatible substances to avoid potential chemical interactions. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087726358746,"sku":"TCI2510M296741419","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2967.jpg?v=1769143006"},{"product_id":"tci2510m312841646","title":"TCI M3128 279262-23-6 4-(Morpholinomethyl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M3128 4-(Morpholinomethyl)phenylboronic Acid, bearing CAS number 279262-23-6 and supplied in a form that contains varying amounts of anhydride, is an organoboron reagent carrying a morpholinomethyl group at the para position of the aromatic ring. In the laboratory, this compound functions as a coupling partner in palladium-catalysed carbon–carbon bond formation, while at the same time serving as a carrier of a cyclic amine group that increases the polarity and solubility of the resulting product. The combination of these two functions within a single reagent is highly valued by medicinal chemists who need to improve the physicochemical properties of candidate molecules without adding extra synthetic steps.\u003c\/p\u003e\n\u003cp\u003eThe most prominent characteristic of this material is the morpholine group, a weakly basic amine ring that is widely recognised for improving the aqueous solubility and pharmacokinetic profile of derivative compounds. At the same time, the boronic acid group provides the well-established Suzuki–Miyaura coupling reactivity that synthetic chemists rely upon. It should be understood that aryl boronic acids naturally undergo a dehydration equilibrium to form boroxines, so the statement that the product contains varying amounts of anhydride is a normal property of this compound class rather than an indicator of poor quality. The advantage of this reagent therefore lies in the way a single building block delivers both a reliable coupling handle and a solubilising motif.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this type are typically found in university and institutional research groups working on organic synthesis, medicinal chemistry, and the preparation of biologically active molecules. They are used at the bench scale for constructing biaryl frameworks, for preparing intermediates required in structure–activity relationship studies, and for supporting postgraduate research projects. Because the material is a specialist building block rather than a bulk chemical, it is usually ordered against a defined synthetic plan and drawn upon in small portions across a series of trial reactions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the boronic acid group transfers the aryl unit to an organohalide partner under palladium catalysis, making it a direct route to biaryl structures.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block: the morpholine ring is introduced together with the aryl unit, letting chemists improve polarity and solubility without adding a separate functionalisation step.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship studies: the reagent allows a morpholinomethylphenyl fragment to be installed on several scaffolds, so researchers can compare how the same substituent affects different molecular series.\u003c\/li\u003e\n\u003cli\u003eSynthesis of biologically active intermediates: the weakly basic amine ring is a recognised motif for tuning pharmacokinetic behaviour, supporting the preparation of candidate compounds in discovery-stage research.\u003c\/li\u003e\n\u003cli\u003eAcademic and postgraduate organic synthesis research: the reagent supports bench-scale carbon–carbon bond formation experiments in university laboratories investigating aromatic coupling methodology.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 279262-23-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: supplied containing varying amounts of the corresponding anhydride (boroxine), which is characteristic of aryl boronic acids\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered by TCI for this article number\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, kept sealed to limit exposure to atmospheric moisture, since aryl boronic acids readily undergo dehydration to the corresponding anhydride. Glass containers with well-fitting closures are appropriate, and the material should be kept in a dry, well-ventilated chemical store away from strong oxidising agents. Handle the solid in a fume hood using safety glasses, gloves, and a laboratory coat, avoiding dust formation and inhalation. Weigh out only the quantity required and reclose the container promptly to preserve the remainder. Always consult the manufacturer's safety data sheet before use and dispose of residues through the laboratory's chemical waste route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087736352986,"sku":"TCI2510M312841646","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087736385754,"sku":"TCI2510M312841647","price":5200000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M3128.jpg?v=1768361803"},{"product_id":"tci2510n109843975","title":"TCI N1098 1133057-98-3 [9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid is a complex organoboron compound widely used in organic chemistry laboratories. This reagent plays a crucial role in various synthetic reactions, particularly in the construction of carbon-carbon bonds. Its unique structure makes it a valuable component in the development of heterocyclic compounds and boronic acid derivatives. Due to its reactivity and versatility, it is an essential tool for researchers working on advanced molecular synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its ability to react under specific conditions, making it a preferred choice in coupling reactions such as Suzuki and Kumada. Its solubility in organic solvents simplifies the preparation of reaction mixtures, while its stability under controlled conditions ensures reliable results. These properties make it a go-to reagent for laboratories requiring precision and consistency in their synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists for the development of new compounds, including pharmaceuticals and industrial chemicals. Its application spans across research and development in both academic and industrial settings. The compound’s role in creating complex molecular structures is vital for advancing chemical innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where carbon-carbon bond formation is required, due to its reactivity and compatibility with coupling mechanisms.\u003c\/li\u003e\n\u003cli\u003eDevelopment of heterocyclic compounds, as its structure allows for the formation of complex ring systems in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research, where it is used to synthesize boronic acid derivatives for drug development and chemical innovation.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production, as it contributes to the creation of boron-containing compounds used in various applications.\u003c\/li\u003e\n\u003cli\u003eAdvanced molecular synthesis projects, where its unique reactivity supports the construction of complex organic molecules.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1133057-98-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Keep in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to incompatible substances, and ensure that storage conditions are consistent with standard laboratory safety protocols. Proper labeling and storage are essential to ensure safe handling and long-term usability in research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087860216026,"sku":"TCI2510N109843975","price":3837000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N1098.jpg?v=1769143156"},{"product_id":"tci2510o070945163","title":"TCI O0709 83145-77-1 Sodium Bis(oxalato)borate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSodium Bis(oxalato)borate, often abbreviated as NaBOB, is a sodium salt in which a central boron atom is chelated by two oxalate ligands to form the bis(oxalato)borate anion. In the TCI catalogue, this compound is classified under main-group element chemistry within the Catalysis and Inorganic Chemistry category. In the laboratory, NaBOB is known mainly as a candidate electrolyte salt and additive in sodium-ion battery research. It parallels its lithium analogue, lithium bis(oxalato)borate, which has been studied extensively in lithium-ion battery systems.\u003c\/p\u003e\n\u003cp\u003eResearchers are interested in NaBOB because its anion contains no fluorine, unlike many conventional electrolyte salts based on hexafluorophosphate. This makes it relevant to the search for more environmentally friendly electrolytes. It may also be more stable against the formation of hazardous by-products such as hydrogen fluoride. Researchers also study the role of the bis(oxalato)borate anion in forming interfacial layers on electrode surfaces, which strongly affect cell performance and lifetime. Its boron–oxalate chelate structure also makes it a useful material for studies of boron coordination chemistry, so its value extends beyond electrochemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, energy storage and battery research is growing quickly, driven by the national push toward electric vehicles and renewable energy. Sodium-ion batteries are attracting attention as a possible complement to lithium-ion technology. University chemistry and materials science departments, government research institutes, and industrial R\u0026amp;D laboratories working on electrolyte formulation can use NaBOB in exploratory studies. Inorganic and coordination chemistry groups can also use it as a well-defined boron chelate compound for teaching and research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSodium-ion battery electrolyte research: NaBOB is studied as a candidate electrolyte salt, which lets researchers evaluate fluorine-free sodium electrolyte formulations in experimental cells.\u003c\/li\u003e\n\u003cli\u003eElectrolyte additive studies: Researchers add the bis(oxalato)borate anion to electrolytes to study how it changes cell behaviour, following the approach already well documented for its lithium analogue in lithium-ion systems.\u003c\/li\u003e\n\u003cli\u003eElectrode interface investigations: The anion is studied for its role in forming interfacial layers on electrode surfaces, so NaBOB suits experiments on how these surface films form and how they behave.\u003c\/li\u003e\n\u003cli\u003eFluorine-free electrolyte development: Because its anion contains no fluorine, NaBOB is relevant to work on greener electrolytes that may avoid hazardous by-products such as hydrogen fluoride.\u003c\/li\u003e\n\u003cli\u003eBoron coordination chemistry: Its chelate structure, with two oxalate ligands around a boron centre, makes it a useful model compound for academic studies of boron coordination and main-group chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code O0709)\u003c\/li\u003e\n\u003cli\u003eCAS number: 83145-77-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Main-group Elements\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in TCI standard pack sizes; please confirm the current options when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: Please refer to the TCI product specification and Certificate of Analysis\u003c\/li\u003e\n\u003cli\u003eStorage: Follow the storage conditions on the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Sodium Bis(oxalato)borate in its original, tightly closed container, in a cool, dry, well-ventilated place away from moisture and incompatible substances. Electrolyte salts used in battery research usually need careful protection from moisture, so many laboratories handle and store them under a dry inert atmosphere, such as in a glovebox. Always follow the storage conditions on the TCI label. Wear standard personal protective equipment, including safety glasses, gloves, and a lab coat. Avoid creating or breathing in dust, and avoid contact with skin and eyes. Read the TCI Safety Data Sheet before use, and dispose of waste according to local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087928864986,"sku":"TCI2510O070945163","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0709.jpg?v=1769057260"},{"product_id":"tci2510p175947432","title":"TCI P1759 109299-78-7 5-Pyrimidylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Pyrimidylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex boron-containing compounds. This reagent plays a crucial role in laboratory settings where precision and efficiency in chemical reactions are essential. Its unique structure allows it to participate in various coupling reactions, making it a valuable tool for chemists and researchers. In Indonesia, this compound is frequently utilized in academic and industrial laboratories for the development of new chemical entities and advanced materials.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its ability to form complexes with transition metals, enhancing the efficiency and specificity of chemical reactions. Its stability under certain conditions ensures safe handling and reliable performance in laboratory experiments. Additionally, its reactivity and selectivity make it ideal for applications requiring high precision. These properties make it a go-to reagent for researchers working on complex molecular structures and pharmaceutical compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Pyrimidylboronic Acid is commonly used in both research and educational settings. It supports the development of new drugs and materials, contributing to advancements in pharmacology and chemical engineering. Its relevance extends to academic institutions, where it is used to teach and demonstrate key concepts in organic chemistry and synthetic methodologies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eOrganic Synthesis\u003c\/strong\u003e: This compound is ideal for synthesizing complex organic molecules, especially those involving boron.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSuzuki Coupling Reactions\u003c\/strong\u003e: It is a key reagent in Suzuki reactions, enabling efficient cross-coupling of aryl halides with boronic acids.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHeck Reactions\u003c\/strong\u003e: It supports the formation of carbon-carbon bonds in Heck reactions, which are critical in pharmaceutical synthesis.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePharmaceutical Development\u003c\/strong\u003e: Its role in creating boron-containing compounds makes it valuable in drug discovery and development.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eEducational Research\u003c\/strong\u003e: It is widely used in academic settings to teach and research advanced organic chemistry techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eBrand\u003c\/strong\u003e: TCI\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCAS Number\u003c\/strong\u003e: 109299-78-7\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCategory\u003c\/strong\u003e: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePack Sizes\u003c\/strong\u003e: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePhysical Form\u003c\/strong\u003e: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eStorage Note\u003c\/strong\u003e: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Pyrimidylboronic Acid should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential risks associated with its chemical properties. Proper labeling and storage conditions ensure safe handling and long-term usability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48088071045338,"sku":"TCI2510P175947432","price":557000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48088071078106,"sku":"TCI2510P175947433","price":3029000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1759.jpg?v=1768206099"},{"product_id":"tci2510p200147721","title":"TCI P2001 854952-58-2 9-Phenylcarbazole-3-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-Phenylcarbazole-3-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds. This versatile building block plays a crucial role in laboratory settings where complex molecular structures are being developed. Its unique chemical structure enables it to participate in various coupling reactions, making it an essential reagent for advanced synthetic pathways. This compound is commonly used in research and development projects that require precise molecular modifications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions and its reactivity with a range of reagents, including strong acids and alkali metals. Its ability to undergo coupling reactions, such as Suzuki or Kumada, makes it a preferred choice for chemists working on the synthesis of complex organic molecules. The presence of boronic acid functionality further enhances its utility in creating new compounds with tailored properties. These characteristics make it a reliable and efficient reagent in modern chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-Phenylcarbazole-3-boronic Acid is extensively used in organic chemistry research, especially in academic institutions and research centers. It is particularly relevant for projects focused on the synthesis of heterocyclic compounds and the development of new pharmaceuticals. Its application is widespread in both teaching and research environments, supporting the advancement of chemical sciences in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of Heterocyclic Compounds: This compound is ideal for creating complex ring structures, which are essential in pharmaceutical and material science research.\u003c\/li\u003e\n\u003cli\u003eOrganic Coupling Reactions: Its boronic acid functionality makes it suitable for Suzuki and Kumada couplings, enabling the formation of new carbon-carbon bonds.\u003c\/li\u003e\n\u003cli\u003eDrug Development Projects: It is used in the design and synthesis of novel therapeutic agents, contributing to the discovery of new pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eAdvanced Organic Chemistry Research: Its reactivity and structural versatility support cutting-edge research in synthetic chemistry and molecular design.\u003c\/li\u003e\n\u003cli\u003eTeaching and Learning in Chemistry: It is a valuable tool for demonstrating complex organic reactions and synthetic strategies in academic settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 854952-58-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its potential reactivity with strong acids and alkali metals, it should be handled with appropriate personal protective equipment. Keep the material away from incompatible substances to ensure safe laboratory practices. Regular monitoring of storage conditions is advised to maintain the integrity of the compound. Always follow standard safety protocols when working with reactive chemical building blocks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088090575066,"sku":"TCI2510P200147721","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088090607834,"sku":"TCI2510P200147722","price":7295000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P2001.jpg?v=1767135559"},{"product_id":"tci2510p210547858","title":"TCI P2105 389621-81-2 4-[(1-Pyrrolidinyl)carbonyl]phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-[(1-Pyrrolidinyl)carbonyl]phenylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules involving boron-based reactions. This reagent plays a crucial role in the formation of new bonds through specific reaction mechanisms, making it an essential tool in modern chemical laboratories. Its unique molecular structure, featuring a reactive boronic acid group, allows it to participate in various coupling reactions. This versatility makes it a valuable component in the development of new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and ability to form stable intermediates make it a preferred choice for chemists working on precise and controlled chemical processes. Its capacity to interact with a wide range of organic substrates enhances its utility in synthetic pathways. The presence of the pyrrolidinyl group further increases its functional versatility, enabling it to be used in multiple reaction types. These properties contribute to its popularity in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmaceutical, material science, and environmental chemistry applications. It is frequently employed in experiments requiring high precision and controlled reaction conditions. Its role in synthesizing complex organic structures makes it a key reagent in both teaching and research environments across various scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for synthesizing complex organic molecules due to its reactivity and ability to form stable intermediates in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development for creating novel compounds with specific biological activities and structural properties.\u003c\/li\u003e\n\u003cli\u003eMaterial Science: The compound's unique structure enables it to be used in the development of advanced materials with tailored chemical and physical properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Chemistry: It plays a role in the synthesis of compounds used for environmental monitoring and remediation processes.\u003c\/li\u003e\n\u003cli\u003eTeaching and Research: It is a common reagent in academic settings for demonstrating and conducting advanced organic reactions and synthetic pathways.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 389621-81-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As listed on product packaging\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its reactive nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage should be in a well-ventilated area to minimize the risk of inhalation of any vapors. Avoid contact with incompatible materials to ensure safe handling and long-term stability. Always follow standard laboratory safety protocols when working with this reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088098046170,"sku":"TCI2510P210547858","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48088098078938,"sku":"TCI2510P210547859","price":4468000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P2105.jpg?v=1768206136"},{"product_id":"tci2510p215847918","title":"TCI P2158 952514-79-3 4-(1-Phenyl-1H-benzimidazol-2-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(1-Phenyl-1H-benzimidazol-2-yl)phenylboronic Acid is a specialized organic compound widely used in laboratory settings for its unique reactivity and structural versatility. This compound plays a crucial role in various organic reactions, particularly in the synthesis of complex molecules containing boron. Its application is especially prominent in coupling reactions such as the Suzuki-Miyaura reaction, which is essential for the development of heterocyclic compounds and organic materials. Due to its ability to interact with transition metals and ligands, it is a valuable reagent in both organic and organometallic chemistry research.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity is further enhanced by the presence of varying amounts of anhydride, which influences its behavior in different reaction conditions. This characteristic allows for flexible use in a wide range of synthetic pathways. Its stability under controlled conditions and its ability to participate in catalytic processes make it a preferred choice for researchers aiming for precise and efficient chemical synthesis. The compound's chemical properties ensure its reliability in both academic and industrial laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the development of new materials and the synthesis of complex organic compounds. It is frequently employed in academic and research institutions to support advanced chemical studies and innovation in the field of organic synthesis. Its versatility and effectiveness make it a key component in the toolkit of chemists working on complex molecular structures.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis for creating complex heterocyclic compounds due to its reactivity and structural compatibility.\u003c\/li\u003e\n\u003cli\u003eApplied in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds efficiently in organic material development.\u003c\/li\u003e\n\u003cli\u003eUtilized in organometallic research for its ability to interact with transition metals and ligands in catalytic processes.\u003c\/li\u003e\n\u003cli\u003eEmployed in the development of new chemical materials due to its versatility in forming stable and reactive intermediates.\u003c\/li\u003e\n\u003cli\u003eIntegrated into research projects requiring precise chemical synthesis for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 952514-79-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder (as per product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its performance in reactions. Due to its potential reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling to ensure safety. The compound should not be stored near incompatible materials or in areas with high humidity. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088101421274,"sku":"TCI2510P215847918","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48088101454042,"sku":"TCI2510P215847919","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P2158.jpg?v=1769057486"},{"product_id":"tci2510p216947933","title":"TCI P2169 1001911-63-2 9-Phenylcarbazole-2-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-Phenylcarbazole-2-boronic Acid is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. It serves as a key building block in the creation of complex heterocyclic compounds, playing a crucial role in various chemical reactions. This compound is particularly valuable in the development of new materials, pharmaceuticals, and industrial chemicals due to its unique molecular structure and reactivity. Its presence in the lab supports advanced research in chemistry and related fields, making it an essential tool for scientists and researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound’s ability to participate in specific chemical reactions, such as Suzuki-Miyaura and Heck coupling, makes it a preferred choice for synthetic chemists. Its stability under certain conditions and compatibility with a variety of reaction environments enhance its utility in laboratory applications. These properties allow it to be used effectively in both academic and industrial research, contributing to the synthesis of a wide range of compounds. Its reliability and performance in controlled environments further solidify its importance in modern chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-Phenylcarbazole-2-boronic Acid is commonly used by researchers in the fields of chemistry, pharmacy, and materials science. It is a critical component in the development of new compounds and is frequently employed in academic and research institutions. Its relevance in these contexts underscores its importance as a fundamental reagent in the pursuit of scientific innovation and discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this compound is used to build complex heterocyclic structures due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its role in the development of new drugs, as it contributes to the synthesis of bioactive compounds.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications rely on its ability to form stable chemical bonds, aiding in the creation of advanced organic materials.\u003c\/li\u003e\n\u003cli\u003eAcademic research utilizes this compound for teaching and experimental purposes, supporting the training of future chemists.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production incorporates it in the manufacture of specialty chemicals and polymers due to its structural versatility.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1001911-63-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. As it contains varying amounts of anhydride, it should be handled with care to avoid potential chemical reactions. Proper ventilation is essential when working with this material to ensure a safe laboratory environment. Always follow standard safety protocols, including the use of personal protective equipment, to minimize risks during handling and experimentation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48088102469850,"sku":"TCI2510P216947933","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48088102502618,"sku":"TCI2510P216947934","price":1465000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P2169.jpg?v=1767135834"},{"product_id":"tci2510p228248074","title":"TCI P2282 867044-33-5 4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules that require boron reactivity. This reagent plays a crucial role in laboratory settings where precise control over chemical reactions is essential. Its unique molecular structure enables it to participate in various functional group reactions, making it a versatile tool for chemists. The compound is commonly used in the formation of boron bonds with different functional groups, such as in Suzuki or Kumada coupling reactions.\u003c\/p\u003e\n\u003cp\u003eAs an organoboron reagent, this compound is highly valued for its ability to facilitate the development of pharmaceutical compounds, organic materials, and industrial chemicals. Its molecular structure, which includes phenyl and benzimidazole groups, provides both reactivity and specificity. These characteristics make it ideal for reactions that require stability and controlled reactivity. The compound’s ability to interact with a variety of functional groups enhances its utility in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is frequently used in organic chemistry research, especially in the fields of pharmacy and materials science. Local researchers often rely on it for experiments involving the synthesis of new compounds or the modification of existing ones. Its specific properties make it a preferred choice for applications requiring high precision and controlled reaction conditions. The compound’s role in advancing chemical research in Indonesia underscores its importance in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound's ability to form boron bonds with various functional groups, enhancing reaction efficiency and product yield.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this reagent to develop new drug compounds by facilitating the formation of complex molecular structures through controlled reactions.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications leverage its reactivity to create advanced organic materials with specific functional properties and structural integrity.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on this compound for the synthesis of specialty chemicals that require precise and stable reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesian universities employs this reagent to explore novel synthetic pathways and improve existing chemical methodologies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 867044-33-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the workspace. The compound should be kept away from incompatible substances to prevent any potential chemical reactions. Regular inspection of storage conditions is advised to ensure optimal preservation and safety in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088110334170,"sku":"TCI2510P228248074","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P2282.jpg?v=1768206150"},{"product_id":"tci2510p247848323","title":"TCI P2478 763120-58-7 1H-Pyrazole-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1H-Pyrazole-4-boronic Acid from TCI (product code P2478) is an organoboron reagent with a boronic acid group at the 4-position of a pyrazole ring that has no substituent on nitrogen. In synthesis laboratories it is used mainly as a coupling partner in Suzuki–Miyaura reactions, where it introduces a pyrazol-4-yl unit into aromatic or heteroaromatic molecules. As the product name states, the material contains varying amounts of anhydride. This is the boroxine form, which forms naturally when boronic acids lose water.\u003c\/p\u003e\n\u003cp\u003eThe main strength of this reagent is that it forms carbon–carbon bonds between the pyrazole ring and a wide range of aryl halides under established palladium-catalysed conditions. The pyrazole motif is very important in medicinal chemistry and appears in many kinase inhibitors, so this reagent offers a short, efficient route to these frameworks. The free N–H on the pyrazole ring can also be modified later, for example by alkylation or arylation, which gives chemists more freedom in molecular design. The anhydride content usually does not interfere with coupling, because the boroxine form also reacts under Suzuki conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, this reagent is useful in university organic chemistry laboratories, pharmaceutical research and development groups, and institutions working on heterocyclic synthesis. Researchers who build compound libraries for biological screening can use it to attach pyrazole units to many aryl and heteroaryl scaffolds. It also suits teaching and research projects on palladium-catalysed cross-coupling. 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