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1008506-24-8

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1008506-24-8 Usage

General Description

3-Methoxypyridine-4-boronic acid is an organic compound that consists of a pyridine ring with a boronic acid moiety attached at the 4-position, as well as a methoxy group at the 3-position. This chemical is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is often employed in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds, and is also utilized in the development of novel materials and catalysts. 3-Methoxypyridine-4-boronic acid is a valuable tool for organic chemists and is a versatile reagent in the synthesis of various complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1008506-24-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,5,0 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1008506-24:
(9*1)+(8*0)+(7*0)+(6*8)+(5*5)+(4*0)+(3*6)+(2*2)+(1*4)=108
108 % 10 = 8
So 1008506-24-8 is a valid CAS Registry Number.

1008506-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxypyridine-4-boronic acid

1.2 Other means of identification

Product number -
Other names (3-methoxypyridin-4-yl)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:1008506-24-8 SDS

1008506-24-8Relevant articles and documents

Preparation method of 2,3'-dimethoxy-[2,4']bipyridine

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Paragraph 0025, (2019/08/20)

The invention discloses a preparation method of 2,3'-dimethoxy-[2,4']bipyridine. The preparation method comprises the following steps: performing a reaction on 3-methoxypyridine and a reagent A underthe alkaline conditions at -100 to 80 DEG C so as to obtain 3-methoxy-4-R-pyridine, and performing a reaction on 3-methoxy-4-R-pyridine and 2-bromo-3-methoxypyridine under the alkaline conditions under the catalysis action of a catalyst at -20 to 180 DEG C so as to prepare 2,3'-dimethoxy-[2,4']bipyridine. The preparation method of 2,3'-dimethoxy-[2,4']bipyridine has the advantages of a high yieldand cheap and easily available raw materials, and is suitable for large-scale production.

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