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106538-35-6

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106538-35-6 Usage

Class

Triazolones

Usage

Medicinal chemistry and drug development

Pharmacological activities

Antibacterial
Antifungal
Antiproliferative

Structure

Triazolone ring system attached to a phenyl group and two bromine atoms

Relevance

Interesting target for further research and development in the pharmaceutical industry due to its structural features and pharmacological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 106538-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,3 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106538-35:
(8*1)+(7*0)+(6*6)+(5*5)+(4*3)+(3*8)+(2*3)+(1*5)=116
116 % 10 = 6
So 106538-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Br2N3O/c15-10-6-7-12(11(16)8-10)19-14(20)17-13(18-19)9-4-2-1-3-5-9/h1-8H,(H,17,18,20)

106538-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dibromophenyl)-5-phenyl-1H-1,2,4-triazol-3-one

1.2 Other means of identification

Product number -
Other names HMS1676F17

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:106538-35-6 SDS

106538-35-6Downstream Products

106538-35-6Relevant articles and documents

Benzohydrazides, Benzothiohydrazides, and Benzamidrazones as Sources of 1,3,4(2H)-Oxadiazolenones, 1,3,4(2H)-Thiadiazolenones, and 1,2,4(5H)-Triazolenones

Barnish, Ian T.,Fung, Shing C.,Gibson, Martin S.,Khan, Saeed R.,Pawalchak, Gordon A.,Tse, Kin M.

, p. 417 - 419 (2007/10/02)

Benzohydrazides, benzothiohydrazides, and benzamidrazones have been converted to 1,3,4(2H)-oxadiazolenones, 1,3,4(2H)-thiadiazolenones, and 1,2,4(5H)-triazolenones respectively by reaction with ethyl chloroformate, with ethyl thiolchlorformate, and with phenyl isocyanate.In some reactions, a carbamate or urea has been isolated as intermediate.

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