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2-({5-nitro-2-pyridinyl}sulfanyl)-1H-benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79134-13-7

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79134-13-7 Usage

Structure

Benzimidazole derivative with a nitro group and a sulfanyl group attached to a pyridinyl ring

Biological activities

Potential as an anti-parasitic agent with inhibitory effects on the growth of various parasites

Therapeutic applications

Potential as a drug candidate for the treatment of parasitic infections

Anti-cancer properties

Has been investigated for its potential anti-cancer properties

Ongoing research

Research on NPSB continues to explore its biological activities and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 79134-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,3 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79134-13:
(7*7)+(6*9)+(5*1)+(4*3)+(3*4)+(2*1)+(1*3)=137
137 % 10 = 7
So 79134-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N4O2S/c17-16(18)8-5-6-11(13-7-8)19-12-14-9-3-1-2-4-10(9)15-12/h1-7H,(H,14,15)

79134-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-nitropyridin-2-yl)sulfanyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names -

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:79134-13-7 SDS

79134-13-7Downstream Products

79134-13-7Relevant academic research and scientific papers

Synthesis and inhibitory effects of 2-pyridyl-2-thiobenzoxazole and 2-pyridyl-2-thiobenzimidazole derivatives on arachidonic acid metabolism

Lagorce,Fatimi,Lakhdar,Chabernaud,Buxeraud,Raby

, p. 1207 - 1210 (2007/10/02)

A series of new 2-pyridyl-2-thiobenzoxazole and 2-pyridyl-2-thiobenzimidazole compounds was prepared and investigated by a number of in vitro methods in order to determine their prostaglandin synthesis inhibitory activity. The most active compound decreases prostaglandin production and carrageenin edema, but has a less platelet antiaggregatory activity.

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