• 2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 365564-10-9) - TCI D5533 - AMI Scientific
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TCI

CAS 365564-10-9

2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI D5533

2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI D5533
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Rp 1.358.700,00
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2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in chemical research, particularly in the synthesis of aromatic and heterocyclic compounds. This reagent plays a crucial role in catalytic reactions, enabling the formation of carbon-carbon bonds with high efficiency. Its application extends to various synthetic pathways, making it an essential component in modern organic chemistry laboratories. Due to its unique molecular structure, it is often employed in advanced synthetic strategies that require precise control over reaction conditions.

The compound is valued for its stability under controlled conditions and its ability to act as a boron hydride source. Its reactivity is particularly notable in transition metal-containing environments, where it facilitates complex organic transformations. The high reactivity and versatility of this reagent make it a preferred choice for researchers aiming to achieve high yields and selectivity in their experiments. Its compatibility with a range of catalysts and reaction conditions further enhances its utility in synthetic chemistry.

In Indonesian laboratories, this compound is commonly used in organic chemistry research and the synthesis of complex molecules. It is a key reagent in the Suzuki-Miyaura coupling reaction, which is widely applied in the development of pharmaceuticals and fine chemicals. Educational and research institutions in Indonesia rely on this product to support experiments requiring specialized reagents for the synthesis of compounds with specific structural features.

  • Suzuki-Miyaura Coupling Reaction for efficient cross-coupling of aryl halides with boronic acids to produce biologically active compounds.
  • Organic Synthesis of Aromatic and Heterocyclic Compounds due to its ability to form carbon-carbon bonds under catalytic conditions.
  • Catalytic Reactions in Transition Metal Systems because of its reactivity in environments containing transition metals.
  • Development of Pharmaceuticals and Fine Chemicals as it enables the synthesis of complex molecular structures with high precision.
  • Research in Organic Chemistry for its role in creating novel compounds with specific functional groups and structural features.

Brand TCI
CAS number 365564-10-9
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid or liquid depending on the formulation
Storage Store in a cool, dry place away from moisture and direct sunlight

This 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 may affect its chemical integrity. Due to its potential reactivity, it should be handled in a well-ventilated laboratory setting, with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper disposal in accordance with local regulations. Regular monitoring of storage conditions is advised to ensure the compound remains suitable for use in chemical reactions.

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