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622864-48-6

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622864-48-6 Usage

General Description

Boronic acid, (3-hydroxy-4-methoxyphenyl)- (9CI) is a chemical compound that belongs to the class of boronic acids. It is characterized by a boronic acid group attached to a 3-hydroxy-4-methoxyphenyl moiety. Boronic acid, (3-hydroxy-4-methoxyphenyl)- (9CI) is used in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of organic compounds. Boronic acids have also been studied for their potential applications in medicinal chemistry, including as inhibitors of enzymes and in the development of new drugs. The specific properties and uses of boronic acid, (3-hydroxy-4-methoxyphenyl)- (9CI) make it an important and versatile compound in various fields of chemistry and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 622864-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,2,8,6 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 622864-48:
(8*6)+(7*2)+(6*2)+(5*8)+(4*6)+(3*4)+(2*4)+(1*8)=166
166 % 10 = 6
So 622864-48-6 is a valid CAS Registry Number.

622864-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Hydroxy-4-methoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (3-hydroxy-4-methoxyphenyl)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:622864-48-6 SDS

622864-48-6Relevant articles and documents

Synthesis and biological evaluation of 4-arylcoumarin analogues of combretastatins. Part 2

Combes, Sébastien,Barbier, Pascale,Douillard, Soazig,McLeer-Florin, Anne,Bourgarel-Rey, Véronique,Pierson, Jean-Thomas,Fedorov, Alexey Yu.,Finet, Jean-Pierre,Boutonnat, Jean,Peyrot, Vincent

experimental part, p. 3153 - 3162 (2011/06/27)

Figure Presented. A series of A-ring variously methoxylated 4-(3-hydroxy-4-methoxyphenyl)coumarins related to combretastatin A-4 was prepared by cross-coupling reactions. Cytotoxicity studies indicated a potent activity against HBL100 cell line. Substitut

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