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2-phenyl-thiazole-4-carbonyl azide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

400775-03-3

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400775-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400775-03-3 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 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 400775-03:
(8*4)+(7*0)+(6*0)+(5*7)+(4*7)+(3*5)+(2*0)+(1*3)=113
113 % 10 = 3
So 400775-03-3 is a valid CAS Registry Number.

400775-03-3SDS

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-phenyl-1,3-thiazole-4-carbonyl azide

1.2 Other means of identification

Product number -
Other names azido-(2-phenyl-1,3-thiazol-4-yl)methanone

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:400775-03-3 SDS

400775-03-3Relevant articles and documents

Five-membered heterocyclic ureas suitable for the donor-donor-acceptor hydrogen-bonding modules

Hisamatsu, Yosuke,Fukumi, Yuki,Shirai, Naohiro,Ikeda, Shin-ichi,Odashima, Kazunori

, p. 2005 - 2009 (2008/09/19)

Five-membered heterocyclic ureas are capable of forming the unfolded conformer without preorganization by using the intramolecular hydrogen bond, and are suitable for the DDA hydrogen-bonding modules. In contrast, six-membered heterocyclic ureas are desta

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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