{"title":"Difluoromethylation [Synthetic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eDifluoromethylation [Synthetic Reagents]\u003c\/strong\u003e — menghimpun reagen berbasis silikon dan ester sulfonat yang membawa gugus difluorometil atau trifluorometil reaktif, dirancang untuk mentransfer unit fluor-karbon ke dalam molekul target melalui reaksi substitusi atau adisi nukleofilik.\u003c\/p\u003e\u003cp\u003eDifluoromethylation [Synthetic Reagents] digunakan kimiawan sintetik untuk memasukkan gugus difluorometil atau trifluorometil ke dalam senyawa aromatik maupun alifatik, baik melalui reaksi dengan nukleofil silikon terkatalis fluorida maupun melalui pembentukan ester teraktivasi, sebagai bagian dari strategi fluorinasi pada pengembangan molekul organik dan bahan antara.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t438256143\"\u003eTCI T4382 1885-46-7 Difluoromethyl Trifluoromethanesulfonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c099115361\"\u003eTCI C0991 1895-39-2 Sodium Chlorodifluoroacetate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t302254534\"\u003eTCI T3022 120801-75-4 Trimethylsilyl Difluoro(fluorosulfonyl)acetate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c145816024\"\u003eTCI C1458 383-62-0 Ethyl Chlorodifluoroacetate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t157052788\"\u003eTCI T1570 81290-20-2 (Trifluoromethyl)trimethylsilane [Trifluoromethylating Reagent]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c150316088\"\u003eTCI C1503 2834-23-3 Chlorodifluoroacetic Anhydride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t133652464\"\u003eTCI T1336 2923-18-4 Sodium Trifluoroacetate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c158616222\"\u003eTCI C1586 1514-87-0 Methyl Chlorodifluoroacetate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jenis gugus pereaksi (trimetilsilil, ester sulfonat, atau turunan asetat terfluorinasi) serta kestabilan reagen agar sesuai dengan kondisi reaksi yang direncanakan. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Fluorination Reagents [Synthetic Reagents], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-fluorination-reagents-other-synthetic-reagents\"\u003eFluorination Reagents (Other) [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-fluorination-synthetic-reagents\"\u003eFluorination [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-trifluoromethylation-synthetic-reagents\"\u003eTrifluoromethylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-trifluoromethylthiolation-synthetic-reagents\"\u003eTrifluoromethylthiolation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-fluorination-reagents-synthetic-reagents\"\u003eFluorination Reagents [Synthetic Reagents]\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510c099115361","title":"TCI C0991 1895-39-2 Sodium Chlorodifluoroacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0991 Sodium Chlorodifluoroacetate (CAS 1895-39-2) is a solid fluorinated building block widely used as an in-situ difluorocarbene source. On heating it enables gem-difluorocyclopropanation of alkenes and difluoromethylation of nucleophiles such as phenols, thiols and amines. AMI Scientific offers this TCI product in 25 g, 100 g and 500 g pack sizes to suit exploratory through repeated synthetic work. Keep the container tightly closed, ensure adequate venting during heated reactions, and follow the manufacturer's label and safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMehta et al. (2014). ChemInform Abstract: S‐, N‐, and Se‐Difluoromethylation Using Sodium Chlorodifluoroacetate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201410085\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201410085\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMehta et al. (2013). S-, N-, and Se-Difluoromethylation Using Sodium Chlorodifluoroacetate. \u003cem\u003eOrganic Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ol402370f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ol402370f\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWilliams et al. (2015). ChemInform Abstract: Mild Chlorodifluoroacylation of Indoles via Self‐Activation of Sodium Chlorodifluoroacetate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201505133\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201505133\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086042378458,"sku":"TCI2510C099115361","price":1603000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086042411226,"sku":"TCI2510C099115362","price":4695000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086042443994,"sku":"TCI2510C099115363","price":15571000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0991.jpg?v=1771058100"},{"product_id":"tci2510c145816024","title":"TCI C1458 383-62-0 Ethyl Chlorodifluoroacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1458 Ethyl Chlorodifluoroacetate (CAS 383-62-0) is a fluorinated ester valued as a practical difluorocarbene precursor. Under suitable conditions it enables difluoromethylation of oxygen, nitrogen, and sulfur nucleophiles, and it also serves directly as a gem-difluoro building block. These transformations are widely applied in pharmaceutical and agrochemical research, where fluorine substitution modulates lipophilicity and metabolic stability. AMI Scientific supplies this TCI product in 25 g and 500 g packs; keep it tightly sealed and protected from moisture as directed by the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBlanco et al. (2016). Atmospheric sink of methyl chlorodifluoroacetate and ethyl chlorodifluoroacetate: temperature dependent rate coefficients, product distribution of their reactions with Cl atoms and CF 2 ClC(O)OH formation. \u003cem\u003eRSC Advances\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c6ra03454c\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c6ra03454c\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBEGUE et al. (1995). ChemInform Abstract: Synthesis of 3‐gem‐Difluoro‐2‐ethoxy Allylic Alcohols from Ethyl Chlorodifluoroacetate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199501093\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199501093\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBégué dkk. (1994). Synthesis of 3-gem-difluoro-2-ethoxy allylic alcohols from ethyl chlorodifluoroacetate. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0040-4039(94)88085-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0040-4039(94)88085-9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086071148762,"sku":"TCI2510C145816024","price":1969000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086071181530,"sku":"TCI2510C145816025","price":18523000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1458.jpg?v=1768204602"},{"product_id":"tci2510c150316088","title":"TCI C1503 2834-23-3 Chlorodifluoroacetic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1503 Chlorodifluoroacetic Anhydride is a highly reactive fluorinated acid anhydride used as a powerful acylating agent for alcohols, amines, and phenols. It transfers the chlorodifluoroacetyl fragment efficiently and also serves as an entry point to difluorocarbene chemistry and difluorinated motifs in medicinal and agrochemical research. Its halogenated acyl group is additionally valuable for analytical derivatization, improving volatility and detector response in gas chromatography. AMI Scientific offers this TCI reagent in 10 g and 25 g packs; because it reacts rapidly with moisture, it must be handled with dry, inert-atmosphere technique in strict accordance with the manufacturer's Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKawamura et al. (2018). Reactivity and properties of bis(chlorodifluoroacetyl) peroxide generated in situ from chlorodifluoroacetic anhydride for chlorodifluoromethylation reactions. \u003cem\u003eChemical Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c8cc05905e\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c8cc05905e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48086074097882,"sku":"TCI2510C150316088","price":2025000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086074130650,"sku":"TCI2510C150316089","price":3542000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1503.jpg?v=1769180351"},{"product_id":"tci2510c158616222","title":"TCI C1586 1514-87-0 Methyl Chlorodifluoroacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1586 Methyl Chlorodifluoroacetate (CAS 1514-87-0) is a widely used fluorinated building block and a practical precursor for generating difluorocarbene. It enables the introduction of difluoromethylene and difluoromethyl motifs into target molecules, supporting pharmaceutical, agrochemical, and functional materials research. Typical uses include difluoromethylation of phenols and thiols as well as the preparation of fluorinated cyclopropanes. AMI Scientific supplies this TCI reagent in 5 g and 25 g packages; please observe the handling precautions in the official TCI Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSU et al. (1992). ChemInform Abstract: Methyl Chlorodifluoroacetate. A Convenient Trifluoromethylating Agent.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199231150\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199231150\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDe-Bao et al. (1991). Methyl chlorodifluoroacetate a convenient trifluoromethylating agent. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0040-4039(91)80566-o\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0040-4039(91)80566-o\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBlanco et al. (2016). Atmospheric sink of methyl chlorodifluoroacetate and ethyl chlorodifluoroacetate: temperature dependent rate coefficients, product distribution of their reactions with Cl atoms and CF 2 ClC(O)OH formation. \u003cem\u003eRSC Advances\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c6ra03454c\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c6ra03454c\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086079701210,"sku":"TCI2510C158616222","price":732000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086079733978,"sku":"TCI2510C158616223","price":1799000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1586.jpg?v=1768204608"},{"product_id":"tci2510d654527584","title":"TCI D6545 185739-14-4 2,2-Difluoroethenyl 4-Methylbenzene-1-sulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2-Difluoroethenyl 4-Methylbenzene-1-sulfonate is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a fluorinated building block, it serves as a key reagent in the development of complex molecules with specific fluorine-containing structures. Its role in the laboratory is critical for creating stable covalent bonds during synthetic processes. This compound is particularly valued for its ability to participate in a variety of chemical transformations, making it a versatile tool for chemists working on advanced synthesis projects.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique properties stem from the presence of fluorine atoms, which significantly influence its reactivity and polarity. These characteristics allow for more precise and efficient chemical reactions, enabling researchers to achieve desired outcomes with greater control. The fluorine atoms also contribute to the molecule’s stability, which is essential in maintaining reaction conditions and preventing unwanted side reactions. This combination of reactivity and stability makes it a preferred choice for applications requiring high specificity and reliability.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly utilized in organic chemistry research, especially in academic and research institutions. It is frequently employed in projects focused on fluorinated compound synthesis, including pharmaceutical and materials science applications. Its role in drug development is particularly significant due to the reactivity and structural versatility it offers. Researchers in Indonesia rely on this compound for its consistent performance and compatibility with various synthetic methodologies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFluorinated Compound Synthesis: This compound is ideal for creating fluorinated molecules due to its reactivity and structural versatility, enabling precise control over molecular design.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in academic and research settings for developing new compounds with specific functional groups and properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its ability to participate in complex reactions makes it valuable in the synthesis of potential drug candidates with enhanced stability and bioavailability.\u003c\/li\u003e\n\u003cli\u003eMaterials Science Innovation: The compound supports the creation of advanced materials with unique chemical properties, beneficial for industrial and technological applications.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry Applications: It serves as a reference standard for analytical techniques, ensuring accurate identification and quantification of fluorinated compounds.\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: 185739-14-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\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 direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its fluorinated nature, it may require careful handling to prevent exposure, especially in environments with high humidity or reactive conditions. Always ensure proper ventilation when working with this compound and follow standard laboratory safety protocols to minimize risks. Regular monitoring of storage conditions is advised to ensure long-term stability and usability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086811115738,"sku":"TCI2510D654527584","price":2334000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086811148506,"sku":"TCI2510D654527585","price":7422000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6545.jpg?v=1768205191"},{"product_id":"tci2510f050030358","title":"TCI F0500 1717-59-5 2,2-Difluoro-2-(fluorosulfonyl)acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2-Difluoro-2-(fluorosulfonyl)acetic Acid is a fluorinated building block widely used in organic chemistry for the synthesis of organofluorine compounds. Its unique molecular structure, containing both fluorine and sulfonate groups, makes it a versatile reagent in laboratory settings. This compound is essential for constructing complex molecules that require fluorine substitution to enhance stability or functional properties. It plays a crucial role in the development of new materials and pharmaceuticals by enabling precise chemical modifications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactive nature and the presence of the fluorosulfonyl group contribute to its effectiveness in various synthetic reactions. Its ability to participate in substitution and other chemical transformations under different conditions makes it a preferred choice for chemists. The combination of fluorine and sulfonate functionalities provides both reactivity and stability, allowing for the synthesis of compounds with specific desired properties. This dual functionality is particularly valuable in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,2-Difluoro-2-(fluorosulfonyl)acetic Acid is commonly used in research related to pharmacology and material science. It supports the development of new compounds with applications in healthcare and industrial sectors. Many research institutions and universities in Indonesia rely on this compound to advance their studies and innovation in chemical sciences. Its availability and reliability make it a key component in the chemical research ecosystem.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of fluorinated compounds due to its reactive fluorosulfonyl group and fluorine atoms.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals where fluorine substitution enhances drug stability and bioavailability.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials with specific chemical and physical properties through controlled functionalization.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the synthesis of polymers and coatings with enhanced performance characteristics.\u003c\/li\u003e\n\u003cli\u003eSupport for academic research in chemistry, particularly in the study of fluorinated building blocks and their reactivity.\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: 1717-59-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated 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 or liquid, 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\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 compatible with its chemical properties, such as glass or high-density polyethylene. 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 material to minimize exposure. Laboratory personnel should be trained in safe handling procedures to ensure compliance with standard safety protocols. Regular inspection of storage conditions is advised to prevent degradation or unintended reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087009132762,"sku":"TCI2510F050030358","price":1969000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0500.jpg?v=1768205353"},{"product_id":"tci2510s090850552","title":"TCI S0908 84349-27-9 Sodium Bromodifluoroacetate","description":"\u003cp\u003e\u003cstrong\u003eSodium Bromodifluoroacetate\u003c\/strong\u003e (CAS 84349-27-9) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eHPLC Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial settings.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C2BrF2NaO2\u003c\/li\u003e\n\u003cli\u003eCAS number: 84349-27-9\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(HPLC)(T)\u003c\/li\u003e\n\u003cli\u003eTCI product code: S0908\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e Bromodifluoroacetic Acid Sodium Salt\u003c\/p\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088269390042,"sku":"TCI2510S090850552","price":3598000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088269422810,"sku":"TCI2510S090850553","price":10737000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510S0908.jpg?v=1768206295"},{"product_id":"tci2510b14636744","title":"TCI B1463 667-27-6 Ethyl Bromodifluoroacetate","description":"\u003cp\u003e\u003cstrong\u003eEthyl Bromodifluoroacetate\u003c\/strong\u003e (CAS 667-27-6) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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