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400776-21-8

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400776-21-8 Usage

Structure

Thiazole derivative with a carboxylic acid functional group and a methoxyphenyl ether group

Usage

Often used in pharmacological research and drug development

Potential properties

May have antimicrobial, anti-inflammatory, or other pharmacological activities

Additional research

Necessary to fully understand its potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 400776-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,7,7 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 400776-21:
(8*4)+(7*0)+(6*0)+(5*7)+(4*7)+(3*6)+(2*2)+(1*1)=118
118 % 10 = 8
So 400776-21-8 is a valid CAS Registry Number.

400776-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Methoxy-phenoxymethyl)-thiazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:400776-21-8 SDS

400776-21-8Downstream Products

400776-21-8Relevant articles and documents

A catch-and-release strategy for the combinatorial synthesis of 4-acylamino-1,3-thiazoles as potential CDK5 inhibitors

Larsen, Scott D.,Stachew, Carl F.,Clare, Paula M.,Cubbage, Jerry W.,Leach, Karen L.

, p. 3491 - 3495 (2007/10/03)

Two-dimensional libraries of 4-acylamino-1,3-thiazoles 9 were prepared via Curtius rearrangement of 1,3-thiazole-4-carbonyl azides 6, trapping of the intermediate isocyanates with oxime resin, and thermal regeneration of the isocyanates from the washed resin in the presence of nucleophiles. Several compounds proved to be selective inhibitors of CDK5/p25 versus the closely homologous CDK2/cyclin A enzyme, with the best analogue (43) possessing over 100-fold selectivity.

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