117480-96-3

Usage

Structure

Heterocyclic ring containing nitrogen and sulfur atoms

Type

Triazolothiadiazole amine

Functional Group

Phenyl group attached to the nitrogen atom

Potential Applications

a. Pharmaceutical industry
b. Agricultural industry
c. Drug development
d. Herbicide and pesticide synthesis
e. Building block for complex organic molecules

Relevance

Structural diversity and unique properties

Interest to Researchers

a. Heterocyclic chemistry
b. Medicinal chemistry
c. Synthesis and manipulation in the laboratory

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 113766-05-5 3-p-tolyoxymethyl-4-amino-5-mercapto-(4H)-1,2,4-triazole 
• 940-64-7 2-(4-methylphenoxy)acetic acid 
• 5319-81-3 (5-hydrazino-[1,3,4]thiadiazol-2-yl)-phenyl-amine 
• 117480-92-9 1-(3-Mercapto-5-p-tolyloxymethyl-[1,2,4]triazol-4-yl)-3-phenyl-thiourea 

Relevant academic research and scientific papers

Synthesis and fungicidal activities of some 3-aryloxymethyl-6-substituted-1,2,4-triazolothiadiazoles

Several 3-aryloxymethyl-1,2,4-triazoles (II and IV) and 3-aryloxymethyl-6-substituted-1,2,4-triazolothiadiazoles (III, V and VI) have been synthesised and screened for their antifungal activities against Aspergillus flavus and Aspergillus niger.

Synthesis and fungicidal activities of some 3-substituted-6-arylamino-1,2,4-triazolo-1,3,4-thiadiazoles

Several 3-substituted-6-arylamino-1,2,4-triazolo-1,3,4-thiadiazoles (III, IV, V and VI) have been synthesized and screened for their antifungal activities against Helminthosporium oryzae and Cephalosporium sacchari.

Synthesis and fungicidal activities of 3-aryloxymethyl-6-substituted-1,2,4-triazolo-1,3,4-thiadiazoles

Several 3-aryloxymethyl-1,2,4-triazoles (II and IV) and 3-aryloxymethyl-6-substituted-1,2,4-triazolo-1,3,4-thiadiazols (III, V and VI) have been synthesised and screened for their antifungal activities against Aspergillus flavus and Aspergillus niger.

A Novel Synthesis of s-Triazolothiadiazole Derivatives

6-Arylamino-3-aryloxymethyl-s-triazolothiadiazoles (III) have been synthesised by the condensation of 4-amino-3-aryloxymethyl-5-mercapto-1,2,4-triazoles (I) with phenyl isothiocyanate.