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863868-32-0

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863868-32-0 Usage

General Description

2-Methyl-5-cyanophenyl boronic acid pinacol ester is a chemical compound primarily used as an organic intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a boron-based reagent that is commonly utilized in Suzuki-Miyaura cross-coupling reactions to create carbon-carbon bonds. 2-METHYL-5-CYANOPHENYL BORONIC ACID PINACOL ESTER is an important tool for organic chemists in the development of new molecules and has potential applications in various fields including medicine, agriculture, and materials science. Its unique structure and reactivity make it a valuable building block in the creation of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 863868-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,6 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 863868-32:
(8*8)+(7*6)+(6*3)+(5*8)+(4*6)+(3*8)+(2*3)+(1*2)=220
220 % 10 = 0
So 863868-32-0 is a valid CAS Registry Number.

863868-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-cyanophenyl boronic acid pinacol ester

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:863868-32-0 SDS

863868-32-0Relevant articles and documents

COMPOUNDS FOR INFLAMMATION AND IMMUNE-RELATED USES

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Paragraph 0097-0098, (2013/05/21)

The invention relates to certain compounds or pharmaceutically acceptable salts, solvates, clathrates, or prodrugs thereof, that are useful as immunosuppressive agents and for treating and preventing inflammatory conditions, allergic disorders, and immune disorders

Process for producing cyano substituted arene boranes and compounds

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Page/Page column 12, (2008/06/13)

A process for producing cyano substituted arene boranes is described. The compounds are useful intermediates to pharmaceutical compounds using the cyano group as a reactant.

Sterically directed functionalization of aromatic C-H bonds: Selective borylation ortho to cyano groups in arenes and heterocycles

Chotana, Ghayoor A.,Rak, Michael A.,Smith, Milton R.

, p. 10539 - 10544 (2007/10/03)

Ir-catalyzed borylations of 4-substituted benzonitriles are described. In contrast to electrophilic aromatic substitutions and directed ortho metalations, C-H activation/borylation enables functionalization at the 2-position, adjacent to the cyano group, when the 4-subsitutent is larger than cyano. When an excess of borane reagent is used, diborylation can be achieved with a single regioisomer being formed in certain cases. Extension of sterically directed borylation to cyano-substituted, five- and six-membered ring heterocycles is also reported.

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