67562-20-3

Basic information

• Product Name: Isobutylboronic acid pinacol ester
• Synonyms: Isobutylboronic acid pinacol ester;(2-Methylpropyl)boronic acid ester;2-Isobutyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;Isobutylboronic acid picol ester
• CAS NO: 67562-20-3
• Molecular Formula: C₁₀H₂₁BO₂
• Molecular Weight: 202.09882
• Mol File: 67562-20-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 192.6±9.0 °C(Predicted)
• Appearance: /
• Density: 0.87±0.1 g/cm3(Predicted)
• Storage Temp.: Refrigerated.
• Solubility: Acetonitrile (Slightly), DMSO (Sparingly), Methanol (Slightly)
• CAS DataBase Reference: Isobutylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: Isobutylboronic acid pinacol ester(67562-20-3)
• EPA Substance Registry System: Isobutylboronic acid pinacol ester(67562-20-3)

Safety Data

• Hazardous Substances Data: 67562-20-3(Hazardous Substances Data)

Usage

General Description

Isobutylboronic acid pinacol ester is a chemical compound that is commonly used in organic synthesis. It is a boronic acid derivative with isobutyl and pinacol groups attached to the boron atom. Isobutylboronic acid pinacol ester is known for its ability to participate in various organic reactions, including Suzuki-Miyaura coupling, Negishi coupling, and Sonogashira coupling. It is often used as a reagent in the production of pharmaceuticals, agrochemicals, and materials science. Isobutylboronic acid pinacol ester is a valuable tool in the field of organic chemistry, where it is utilized to create complex molecular structures and functionalize organic molecules.

Downstream Products

• 1220099-38-6 C₂₇H₄₄BrN₃O₃ 
• 1338073-39-4 (R)-2-(1-(4-methoxyphenyl)-5-methylhexan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 872309-99-4 5-methyl-1-phenylhexan-3-ol 
• 84110-34-9 2-(2-methylpropyl)-(3aS,4S,6S,7aR)-hexahydro-3a,5,5-trimethyl-4,6-methano-1,3,2-benzodioxaborole 

Relevant articles and documents

ALPHA-AMINOBORONIC ACID DERIVATIVES

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