225659-02-9

Basic information

• Product Name: 1-<4-(benzoylamino)benzoyl>-4-phenylsemicarbazide
• CAS NO: 225659-02-9
• Molecular Weight: 374.399
• Mol File: 225659-02-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-<4-(benzoylamino)benzoyl>-4-phenylsemicarbazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<4-(benzoylamino)benzoyl>-4-phenylsemicarbazide(225659-02-9)
• EPA Substance Registry System: 1-<4-(benzoylamino)benzoyl>-4-phenylsemicarbazide(225659-02-9)

Safety Data

• Hazardous Substances Data: 225659-02-9(Hazardous Substances Data)

Upstream product

• 103-71-9 phenyl isocyanate 
• 146305-29-5 N-[4-(hydrazinylcarbonyl)phenyl]benzamide 

Downstream Products

• 225659-03-0 5-(4-aminophenyl)-2,4-dihydro-4-phenyl-3H-1,2,4-triazol-3-one 

Relevant articles and documents

Synthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates

Ethyl 2-arylhydrazono-3-oxobutyrates 6a-f, 5-(4-aminophenyl)-2,4-dihydro-4-phenyl-3H-1,2,4-triazol-3-one 5d and 1--4-phenylsemicarbazide 4d were synthesized in order to determine their antimicrobial properties. Their structures were elucidated using spectral data. The synthesized compounds were tested in vitro against one Gram-positive and 2 Gram-negative bacterial strains, one Mycobacterial strain and a fungus Candida albicans. Compound 6d showed significant activity against Staphylococcus aureus whereas the others had no remarkable activity on this strain. Compound 6e was found to be more active than the others against Mycobacterium fortuitum at a MIC value of 32 μg/ml. The antibacterial and antifungal activities of 4d, 5d and 6a-f were also compared with various standard drugs. - Keywords: 1,2,4-triazolin-3-ones; 1,2,4-triazoline-3-thiones; semicarbazides; coupling products; microdilution method