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107037-21-8

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107037-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107037-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,3 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107037-21:
(8*1)+(7*0)+(6*7)+(5*0)+(4*3)+(3*7)+(2*2)+(1*1)=88
88 % 10 = 8
So 107037-21-8 is a valid CAS Registry Number.

107037-21-8SDS

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 2-amino-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)purine

1.2 Other means of identification

Product number -
Other names 9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-2-aminopurine

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:107037-21-8 SDS

107037-21-8Upstream product

107037-21-8Relevant articles and documents

Photochemical Behavior of 2-Azidopurine Tri-O-Acetylribonucleoside in Aqueous Solution: Unprecedented Transformation into 1-(5′-O-Acetyl-β-D-Ribofuranosyl)-5-[(2-Oxo-1,3,5-Oxadiazocan-4-Ylidene)Amino]-1 H-Imidazole-4-Carbaldehyde

Komodziński, Krzysztof,Gdaniec, Zofia,Skalski, Bohdan

, p. 235 - 245 (2015/03/30)

The photochemical behavior of 2-azidopurine 2′,3′,5′-tri-O-acetylribonucleoside has been investigated in aqueous solution under aerobic and anaerobic conditions. The two major processes under anaerobic irradiation of 2-azidopurine 2′,3′,5′-tri-O-acetylribonucleoside involve unprecedented transformation into 1-(5′-O-acetyl-β-D-ribofuranosyl)-5-[(2-oxo-1,3,5-oxadiazocan-4-ylidene)amino]-1H-imidazole-4-carbaldehyde and photoreduction to respective 2-aminopurine derivative, whereas under aerobic conditions these two processes occur to a much lesser extent and photooxidation to respective 2-nitropurine derivative dominates. The structures of photoproducts formed were confirmed by NMR and high-resolution electrospray ionization mass spectral data.

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