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73768-75-9

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73768-75-9 Usage

Molar mass

295.31 g/mol

Structure

A complex molecule with a nitro group attached to a pyridine ring and a benzimidazole ring.

Use in pharmaceutical and research applications

Yes, particularly in the development of new drugs and treatments.

Specific properties and potential uses

Currently under investigation, may have applications in medicinal chemistry, biochemistry, and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 73768-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,6 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73768-75:
(7*7)+(6*3)+(5*7)+(4*6)+(3*8)+(2*7)+(1*5)=169
169 % 10 = 9
So 73768-75-9 is a valid CAS Registry Number.

73768-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-nitropyridin-2-yl)sulfanyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names <Nitro-3-Pyridyl-2>-<Benzimidazolyl-2>-Thioaether

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:73768-75-9 SDS

73768-75-9Relevant articles and documents

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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