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6-Methylpyridine-2-boronic acid is a chemical compound that is frequently utilized in scientific research, particularly within the realm of organic chemistry. This boronic acid derivative of pyridine is classified as a boronic acid and possesses the molecular formula C6H8BNO2. It is recognized as a potent agent in chemical synthesis, playing a vital role in the Suzuki coupling, a widely-used type of palladium-catalyzed coupling reaction. It is commonly employed as a reagent or catalyst to facilitate a variety of chemical reactions. However, due to its potential hazards, it is essential to handle this chemical substance with caution.

372963-50-3

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372963-50-3 Usage

Uses

Used in Organic Chemistry Research:
6-Methylpyridine-2-boronic acid is used as a reagent in the field of organic chemistry for its ability to participate in various chemical reactions, including the Suzuki coupling. This reaction is a significant method for the formation of carbon-carbon bonds, which is crucial for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Methylpyridine-2-boronic acid is used as a catalyst to facilitate the synthesis of new drug molecules. Its role in the Suzuki coupling reaction allows for the creation of diverse molecular structures, which can be essential in the development of novel therapeutic agents.
Used in Material Science:
6-Methylpyridine-2-boronic acid is also utilized in material science as a component in the synthesis of new materials with specific properties. The versatility of the Suzuki coupling reaction it participates in enables the creation of materials with tailored characteristics for various applications, such as electronics or advanced materials.
Used in Academic Research:
6-Methylpyridine-2-boronic acid is employed as a research tool in academic institutions, where it is used to study the mechanisms of chemical reactions and to explore new synthetic pathways. Its involvement in the Suzuki coupling reaction provides a platform for understanding the intricacies of palladium-catalyzed coupling processes.

Check Digit Verification of cas no

The CAS Registry Mumber 372963-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,9,6 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 372963-50:
(8*3)+(7*7)+(6*2)+(5*9)+(4*6)+(3*3)+(2*5)+(1*0)=173
173 % 10 = 3
So 372963-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BNO2/c1-5-3-2-4-6(8-5)7(9)10/h2-4,9-10H,1H3

372963-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-Methylpyridin-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 6-Methylpyridine-2-boronic acid

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:372963-50-3 SDS

372963-50-3Upstream product

372963-50-3Downstream Products

372963-50-3Relevant academic research and scientific papers

BI-ARYL AMINOTETRALINES

-

Page/Page column 17, (2010/03/04)

The invention is concerned with the compounds of formula I: and pharmaceutically acceptable salts and esters thereof, wherein R1-R5, A, B, Q, W, and X are defined in the detailed description and claims. In addition, the present invention relates to methods of manufacturing and using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds of formula I are antagonists at the CRTH2 receptor and may be useful in treating diseases and disorders associated with that receptor such as asthma.

Improved synthesis of azaheteroarylboronic acids using tris-trimethylsilylborate under mild conditions

Matondo, Hubert,Souirti, Souad,Baboulene, Michel

, p. 795 - 800 (2007/10/03)

A new family of azaheteroarylboronic acids was synthesized with good yields (70% to 75%). The proposed strategy utilizes an improved transmetalation reaction from Grignard azine reagents and tris-trimethylsilylborate, little used until now.

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