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19765-60-7

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19765-60-7 Usage

Chemical compound

6-Chloropurine 3-oxide

Classification

Purine derivative

Usage

Potent mutagen used in research to induce mutations in bacterial and mammalian cells

Reactivity

Highly reactive compound

Applications

Studies of DNA repair mechanisms and mutation rates

Mutagenic properties

Induces high frequency of base-pair substitutions and frameshift mutations

Safety precautions

Handle with caution and follow proper safety protocols when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 19765-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19765-60:
(7*1)+(6*9)+(5*7)+(4*6)+(3*5)+(2*6)+(1*0)=147
147 % 10 = 7
So 19765-60-7 is a valid CAS Registry Number.

19765-60-7SDS

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 6-chloro-3-hydroxypurine

1.2 Other means of identification

Product number -
Other names 6-Chlor-purin-3-N-oxid

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:19765-60-7 SDS

19765-60-7Upstream product

19765-60-7Downstream Products

19765-60-7Relevant articles and documents

Purines. LXVIII. Trifluoroperoxyacetic acid oxidation of N6-benzyladenine: Formation of the N(3)-oxide and N(7)-oxide, and their cytokinin activities

Fujii,Takada,Ogawa,Itaya,Matsubara

, p. 325 - 327 (1995)

Treatment of N6-benzyladenine (2) with 15% aqueous H2O2 in trifluoroacetic acid at 65-70°C for I h was found to give the N(3)-oxide (3) and the N(7)-oxide (4) in 4% and 4% yields, respectively. The structure of 3 was estab

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