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6-Chloro-5-Methylpyridine-3-Boronic Acid, Pinacol Ester is a chemical compound belonging to the classes of pyridines and boronic acids and their derivatives. It is a crystalline solid that is commonly used in organic synthesis, particularly for the preparation of pharmaceutical and biologically active compounds. The presence of the boronic ester group (Pinacol Ester) makes it a versatile compound for Suzuki-Miyaura cross-coupling reactions, which are widely used in organic chemistry for the formation of carbon-carbon bonds. Due to potential health hazards, handling of this substance requires caution.

1010101-07-1

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1010101-07-1 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-5-Methylpyridine-3-Boronic Acid, Pinacol Ester is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to participate in Suzuki-Miyaura cross-coupling reactions allows for the creation of diverse and complex molecular structures, contributing to the development of new drugs with improved therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 6-Chloro-5-Methylpyridine-3-Boronic Acid, Pinacol Ester is used as a reagent for the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for constructing molecular frameworks and is particularly useful in the synthesis of natural products, agrochemicals, and other biologically active molecules.
Used in Research and Development:
6-Chloro-5-Methylpyridine-3-Boronic Acid, Pinacol Ester is utilized in research and development for the exploration of new synthetic routes and methodologies. Its unique reactivity and compatibility with various coupling partners make it a valuable compound for studying reaction mechanisms and developing novel strategies in organic chemistry.
Used in the Synthesis of Biologically Active Compounds:
6-Chloro-5-Methylpyridine-3-Boronic Acid, Pinacol Ester is employed as a building block in the synthesis of biologically active compounds, such as agrochemicals and other bioactive molecules. Its ability to form carbon-carbon bonds through cross-coupling reactions enables the creation of diverse structures with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1010101-07-1 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 1010101-07:
(9*1)+(8*0)+(7*1)+(6*0)+(5*1)+(4*0)+(3*1)+(2*0)+(1*7)=31
31 % 10 = 1
So 1010101-07-1 is a valid CAS Registry Number.

1010101-07-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H27582)  2-Chloro-3-methylpyridine-5-boronic acid pinacol ester, 95%   

  • 1010101-07-1

  • 250mg

  • 1862.0CNY

  • Detail
  • Alfa Aesar

  • (H27582)  2-Chloro-3-methylpyridine-5-boronic acid pinacol ester, 95%   

  • 1010101-07-1

  • 1g

  • 4434.0CNY

  • Detail

1010101-07-1SDS

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-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER

1.2 Other means of identification

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

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:1010101-07-1 SDS

1010101-07-1Downstream Products

1010101-07-1Relevant 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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