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9-(2-O-pentanoyl-beta-D-arabinofuranosyl)-9H-purin-6-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87970-07-8

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87970-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87970-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,7 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87970-07:
(7*8)+(6*7)+(5*9)+(4*7)+(3*0)+(2*0)+(1*7)=178
178 % 10 = 8
So 87970-07-8 is a valid CAS Registry Number.

87970-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(2-O-valeryl-β-D-arabinofuranosyl)adenine

1.2 Other means of identification

Product number -
Other names Pentanoic acid (2R,3S,4R,5R)-2-(6-amino-purin-9-yl)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-3-yl ester

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:87970-07-8 SDS

87970-07-8Downstream Products

87970-07-8Relevant academic research and scientific papers

Synthesis and evaluation of a series of 2'-O-acyl derivatives of 9-β-D-arabinofuranosyladenine as antiherpes agents

Baker,Kumar,Waites,Arnett,Shannon,Higuchi,Lambert

, p. 270 - 274 (1984)

A series of four 9-(2-O-acyl-β-D-arabinofuranosyl)adenines was synthesized by acylation of 9-[3,5-bis-O-(tert-butyldimethylsilyl)-β-D-arabinofuranosyl]adenine followed by removal of the tert-butyldimethylsilyl groups under conditions (HOAc, teta-N-butyammonium fluoride) that prevented acyl migration. The four 2'-O-acyl derivatives showed activity in vitro against herpes type 1 viruses [virus ratings = 1.5-2.6; MIC50 = 26-72 μg/mL (8.48-21.3 x 10-5 M)]. The 2'-O-acetyl (5a) and 2'-O-valeryl derivatives were evaluated in a guinea pig model for genital herpes (herpes type 2); only 5a showed potent activity when given 6 or 24 h postinfection.

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