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302964-20-1

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302964-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302964-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 302964-20:
(8*3)+(7*0)+(6*2)+(5*9)+(4*6)+(3*4)+(2*2)+(1*0)=121
121 % 10 = 1
So 302964-20-1 is a valid CAS Registry Number.

302964-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butoxycarbonylamino-1,3-thiazole-5-carboxylic acid chloride

1.2 Other means of identification

Product number -
Other names 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylic 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:302964-20-1 SDS

302964-20-1Relevant articles and documents

Scalable and impurity-free process for dasatinib: Src and BCR-Abl inhibitor

Buchappa,Sagar Vijay Kumar,Durga Prasad,Aparna

, p. 1621 - 1628 (2018/06/12)

An efficient, telescopic, impurity-free and scalable process for Bcr-Abl and Src family tyrosine kinase inhibitor for synthesis of Dasatinib with high yield and purity is described.

A convenient new and efficient commercial synthetic route for dasatinib (Sprycel)

Suresh, Garbapu,Nadh, Ratnakaram Venkata,Srinivasu, Navuluri,Yennity, Durgaprasad

, p. 1610 - 1621 (2017/09/08)

A new and efficient synthetic route for dual-Src/Abl kinase inhibitor dasatinib (Sprycel), an anticancer drug, is described. This commercially viable process yields dasatinib monohydrate free of potential impurities with consistent yield of 68% in route A and 61% in route B with HPLC purity >99.80% over four stages.

PYRIDINONE AND PYRIMIDINONE DERIVATIVES AS FACTOR XIA INHIBITORS

-

Page/Page column 253, (2013/07/05)

The present invention provides compounds of the general formula (I), their salts and N- oxides, and solvates and prodrugs thereof (wherein the characters are as defined in the description). The compounds of the general formula (I) are inhibitors of Factor XIa, so that they are useful in the prevention of and/or therapy for thromboembolic diseases.

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