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.

Upstream product

• 5470-18-8 2-Chloro-3-nitropyridine 
• 134469-07-1 Benzimidazol-2-thiol 

Downstream Products

• 157168-69-9 1-[2-(1H-Benzoimidazol-2-ylsulfanyl)-pyridin-3-yl]-3-benzoyl-thiourea 

Relevant academic research and scientific papers

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

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.

A Synthesis of 1,3,5-Thiadiazepine Skeleton Derivatives: Benzimidazopyridothiadiazepine and Benzimidazobenzothiadiazepine Derivatives

Pyrido and benzothiadiazepine derivatives have been successfully synthesized in good yields by the reaction of N-substituted thiourea (6) and N-substituted S-methylisothiourea (7) derivatives in the presence of DCC or potassium carbonate.