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132722-90-8

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132722-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132722-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132722-90:
(8*1)+(7*3)+(6*2)+(5*7)+(4*2)+(3*2)+(2*9)+(1*0)=108
108 % 10 = 8
So 132722-90-8 is a valid CAS Registry Number.

132722-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,4S,5R)-4-fluoro-5-purin-9-yloxolan-2-yl]methanol

1.2 Other means of identification

Product number -
Other names 2'-F-Ara-ddp

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:132722-90-8 SDS

132722-90-8Relevant articles and documents

Enhanced Brain Delivery of an Anti-HIV Nucleoside 2'-F-ara-ddI by Xanthine Oxidase Mediated Biotransformation

Shanmuganathan, Kirupa,Koudriakova, Tatiana,Nampalli, Satyanarayana,Du, Jinfa,Gallo, James M.,et al.

, p. 821 - 827 (2007/10/02)

In order to enhance the brain delivery of 2'-F-ara-ddI, 2'-F-ara-ddP 6 was synthesized and its in vitro and in vivo bioconversion reaction studied.For the study, a new efficient synthetic method for 2'-F-ara-ddP 6 was developed from 5-benzoyl-1,2-O-isopro

Potential Anti-AIDS Drugs. Lipophilic, Adenosine Deaminase-Activated Prodrugs

Barchi, Joseph J.,Marquez, Victor E.,Driscoll, John S.,Ford, Harry,Mitsuya, Hiroaki,et al.

, p. 1647 - 1655 (2007/10/02)

Selected acid-stable (2'-fluoro-2',3'-dideoxyarabinofuranosyl)adenine nucleosides containing methyl groups and other lipophilic functions at various positions in the adenine ring were prepared and evaluated as anti-HIV agents.The N6-methyl (1f)

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