122772-38-7

Basic information

• Product Name: [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-[5-(2-chloro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine
• Synonyms: [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-[5-(2-chloro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine
• CAS NO: 122772-38-7
• Molecular Weight: 334.229
• Mol File: 122772-38-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-[5-(2-chloro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-[5-(2-chloro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(122772-38-7)
• EPA Substance Registry System: [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-[5-(2-chloro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(122772-38-7)

Safety Data

• Hazardous Substances Data: 122772-38-7(Hazardous Substances Data)

Upstream product

• 828-81-9 2-amino-5-(2-chlorophenyl)-1,3,4-thiadiazole 
• 104-88-1 4-chlorobenzaldehyde 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 122772-41-2 2-(2-Chloro-phenyl)-7-(4-chloro-phenyl)-6-phenyl-6,7-dihydro-[1,3,4]thiadiazolo[3,2-a][1,3,5]triazine-5-thione 
• 122772-45-6 2-(2-Chloro-phenyl)-7-(4-chloro-phenyl)-6-o-tolyl-6,7-dihydro-[1,3,4]thiadiazolo[3,2-a][1,3,5]triazine-5-thione 

Relevant articles and documents

Studies on the synthesis and bioactivity of some thiadiazole derivatives

Several 2-aryl-3-(4-aryl-1,3,4-thiadiazolyl)-4-thiazolidinones 3 and several other fused heterocycles 5 have been prepared. Most of the compounds 3 have been screened for their fungicidal activity against two fungi Aspergillus clavatus and Aspergillus fum

(4 + 2) Cycloaddition of conjugated azomethines to aryl isothiocyanates and fungitoxicity of the resulting 6,7-dihydro-1,3,4-thiadiazolo-s-triazine-5(H)-thiones

(4 + 2) Cycloaddition of conjugated azomethines, 5-aryl/aryloxymethyl-2-benzylideneamino-1,3,4-thiadiazoles (3a-l), to aryl isothiocyanates affords 2,6,7-trisubstituted 6,7-dihydro-1,3,4-thiadiazolo-s-triazine-5(H)-thiones (4a-l).The compounds 4a-l have been compared with Dithane M-45, a standard fungicide, for their antifungal activity against A. niger and F. oxysporium.