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1010101-06-0

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1010101-06-0 Usage

Description

2-Chloro-3-methylpyridine-4-boronic acid pinacol ester is a chemical compound that belongs to the group of boronic acid pinacol esters. It is derived from pyridine and contains a chlorine atom and a methyl group on the pyridine ring. 2-CHLORO-3-METHYLPYRIDINE-4-BORONIC ACID PINACOL ESTER is characterized by its boronic acid functionality, which is useful for the formation of carbon-carbon bonds, and its pinacol ester moiety, which provides stability and solubility in organic solvents.

Uses

Used in Organic Synthesis:
2-Chloro-3-methylpyridine-4-boronic acid pinacol ester is used as a reagent for cross-coupling reactions in organic synthesis. Its boronic acid functionality allows for the formation of carbon-carbon bonds, making it a valuable tool in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-chloro-3-methylpyridine-4-boronic acid pinacol ester is used as a building block for the preparation of biologically active molecules. Its unique structure and reactivity make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
2-Chloro-3-methylpyridine-4-boronic acid pinacol ester is also utilized in the agrochemical industry for the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to form carbon-carbon bonds and its stability in organic solvents make it a valuable component in the development of these products.
Used in Academic Research:
In academic research, 2-chloro-3-methylpyridine-4-boronic acid pinacol ester is used for the development of new chemical compounds. Its unique properties and reactivity make it an interesting subject for study, and its potential applications in various fields make it a valuable resource for researchers working on the synthesis and development of novel compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1010101-06-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,1,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1010101-06:
(9*1)+(8*0)+(7*1)+(6*0)+(5*1)+(4*0)+(3*1)+(2*0)+(1*6)=30
30 % 10 = 0
So 1010101-06-0 is a valid CAS Registry Number.

1010101-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2-Chloro-3-methylpyridine-4-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:1010101-06-0 SDS

1010101-06-0Downstream Products

1010101-06-0Relevant articles and documents

A [4+2] cycloaddition strategy to pyridine boronic ester derivatives

Delaney, Patrick M.,Huang, Jianhui,Macdonald, Simon J. F.,Harrity, Joseph P. A.

supporting information; experimental part, p. 781 - 783 (2009/04/07)

Alkynylboronate cycloadditions of 1,4-oxazin-2-ones and 2-pyrazinones provide a direct and regioselective route to functionalized pyridine boronic ester derivatives.

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