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127525-52-4

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127525-52-4 Usage

Chemical class

Triazine derivatives

Industrial applications

a. Intermediate in the synthesis of pharmaceuticals
b. Intermediate in the synthesis of agrochemicals

Chemical structure

a. Triazine ring with a thione functional group at the 6th position
b. 4-chlorophenylmethyl group at the 5th position
c. Phenyl group at the 3rd position

Biological activity

Potential medicinal properties

Research interest

Of interest to researchers for its potential medicinal properties

Check Digit Verification of cas no

The CAS Registry Mumber 127525-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,2 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127525-52:
(8*1)+(7*2)+(6*7)+(5*5)+(4*2)+(3*5)+(2*5)+(1*2)=124
124 % 10 = 4
So 127525-52-4 is a valid CAS Registry Number.

127525-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-Triazine-6(1H)-thione, 5-[(4-chlorophenyl)methyl]-3-phenyl-

1.2 Other means of identification

Product number -
Other names 2(3H)-Oxazolone,5-(4-bromophenyl)

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:127525-52-4 SDS

127525-52-4Relevant articles and documents

Synthesis of some novel N-ribosyl-1,2,4-triazin-6(1H)-/ones or thiones as potential antibacterial and antifungal chemotherapeutics

Khalil, Nasser S. A. M.

, p. 111 - 120 (2007/10/03)

Ribosylation of 3-aryl-5-benzyl(or substituted benzyl)-1,2,4-triazin-6(1H)- /ones or thiones with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose gave the corresponding 3-aryl-5-benzyl(or substituted benzyl)-1-(2,3,5-tri-O-benzoyl- β-D-ribofuranosyl)-1,2,4-triazin-6(1H)-/ones or thiones. The structure of the new ribosides was confirmed chemically and spectroscopically. Copyright

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