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Isobutylboronic acid pinacol ester is a boronic acid derivative featuring isobutyl and pinacol groups attached to the boron atom. It is a versatile chemical compound widely used in organic synthesis for its ability to participate in various organic reactions, such as Suzuki-Miyaura, Negishi, and Sonogashira couplings. Isobutylboronic acid pinacol ester is a valuable tool in organic chemistry, enabling the creation of complex molecular structures and functionalization of organic molecules.

67562-20-3

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67562-20-3 Usage

Uses

Used in Pharmaceutical Industry:
Isobutylboronic acid pinacol ester is used as a reagent for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its ability to participate in various organic reactions allows for the creation of complex molecular structures, enhancing the efficacy and selectivity of pharmaceutical compounds.
Used in Agrochemical Industry:
Isobutylboronic acid pinacol ester is employed as a reagent in the production of agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis enables the development of novel and effective agrochemicals, improving crop protection and yield.
Used in Materials Science:
Isobutylboronic acid pinacol ester is used as a reagent in the synthesis of advanced materials, including polymers, nanoparticles, and other functional materials. Its ability to participate in various organic reactions facilitates the development of innovative materials with unique properties and applications in various fields, such as electronics, energy, and environmental protection.
Used in Organic Synthesis:
Isobutylboronic acid pinacol ester is used as a key intermediate in organic synthesis, enabling the formation of carbon-carbon, carbon-heteroatom, and other important bonds. Its participation in Suzuki-Miyaura, Negishi, and Sonogashira couplings allows for the efficient construction of complex molecular structures, which are essential in the synthesis of natural products, pharmaceuticals, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 67562-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,6 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67562-20:
(7*6)+(6*7)+(5*5)+(4*6)+(3*2)+(2*2)+(1*0)=143
143 % 10 = 3
So 67562-20-3 is a valid CAS Registry Number.

67562-20-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyl-2-(2-methylpropyl)-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names pinacol 2-methylpropane-1-boronate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67562-20-3 SDS

67562-20-3Upstream product

67562-20-3Relevant academic research and scientific papers

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