77712-56-2

Usage

Chemical structure

A heterocyclic organic compound with a triazolo-thiadiazole ring system, a phenyl group, and a chlorophenyl group.

Potential applications

Pharmaceutical uses, including as an antitumor, antifungal, anti-inflammatory, analgesic, and central nervous system depressant agent.

Research status

Further research is needed to fully understand the potential uses and effects of 1,2,4-Triazolo(3,4-b)(1,3,4)thiadiazole, 6-(4-chlorophenyl)-3-phenyl-.

Molecular weight

Not provided in the material.

Solubility

Not provided in the material.

Stability

Not provided in the material.

Reactivity

Not provided in the material.

Synthesis

Not provided in the material.

Toxicity

Not provided in the material.

InChI:InChI=1/C15H9ClN4S/c16-12-8-6-11(7-9-12)14-19-20-13(17-18-15(20)21-14)10-4-2-1-3-5-10/h1-9H

Upstream product

• 22706-11-2 3-phenyl-4-amino-5-mercapto-1,2,4-triazole 
• 74-11-3 para-chlorobenzoic acid 
• 3004-42-0 2-Mercapto-5-phenyl-1,3,4-oxadiazole 
• 56377-34-5 (Z)-3-chloro-3-(4-chlorophenyl)acrylic acid 

Relevant academic research and scientific papers

Unprecedented conversion of (Z)-3-chloro-3-arylacrylic acids to benzoic acids: Synthesis of s-triazolo[3,4-b][1,3,4]thiadiazoles

An unprecedented method for the conversion of (Z)-3-chloro-3-arylacrylic acids to corresponding benzoic acids by stirring in POCl3 at 80 °C is reported. The benzoic acids formed in situ undergo condensation with 4-amino-5-aryl-3-mercapto-1,2,4-

Synthesis and Pharmacology of 2-Aryl/aralkyl-5-aryl/aralkyl/diaralkyl-s-triazolo-1,3,4-thiadiazoles

A series of s-triazolo-1,3,4-thiadiazoles (III) carrying aryl or aralkyl group at 2-position and aryl, aralkyl or diaralkyl group at 5-position have been synthesised and evaluated for their biological activities.Some of the compounds exhibit strong CNS depressant and mild to moderate antiinflammatory action in experimental animals.

Heterocyclic Systems with Bridgehead Nitrogen Atom : Reactions of 4-amino-5-mercapto-3-substituted-s-triazoles with Haloketones, Carboxylic acids and α-halo acids

The reactions of 4-amino-5-mercapto-3-substituted-3-triazoles(I) with chloranil and α-haloketones furnished 3,10-disubstituted-6,13-dichloro,bis(s-triazolothiadiazino)cyclohexa-1,4-diene (II) and 7H-3,6-disubstituted-s-t