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169516-55-6

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169516-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169516-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,1 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169516-55:
(8*1)+(7*6)+(6*9)+(5*5)+(4*1)+(3*6)+(2*5)+(1*5)=166
166 % 10 = 6
So 169516-55-6 is a valid CAS Registry Number.

169516-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-7-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro-β-D-arabinofuranosyl)pyrrolo<2,3-d>pyrimidine

1.2 Other means of identification

Product number -
Other names 4-chloro-7-(2-deoxy-2-fluoro-3,5-di-O-benzoyl-β-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

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:169516-55-6 SDS

169516-55-6Relevant articles and documents

CYCLIC DINUCLEOTIDES AS ANTICANCER AGENTS

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Paragraph 1384; 1387; 1388, (2019/02/13)

The present invention is directed to compounds of the formulae I, II and III as shown below wherein all substituents are defined herein, as well as pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.

ANTIVIRAL AGENTS

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Page/Page column 12, (2012/01/15)

Compounds of structural formula (I): and pharmaceutically acceptable salts thereof; as defined herein, are described for use in the prevention and/or treatment of HCV infections. Novel compounds of the formula (I) and pharmaceutical formulations containin

Chemoselective staudinger strategy in the practical, fit for purpose, gram-scale synthesis of an HCV RNA polymerase inhibitor

Campeau, Louis-Charles,O'Shea, Paul D.

scheme or table, p. 57 - 60 (2011/02/25)

The use of a late-stage selective Staudinger reaction in the preparation of the novel HCV RNA polymerase inhibitor is described. Georg Thieme Verlag Stuttgart - New York.

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