1228009-94-6

Basic information

• Product Name: 1-[(4-benzoyl-5-phenyl-1-p-methoxyphenyl-1H-pyrazol-3-yl)carbonyl]-1-phenylsemicarbazide
• CAS NO: 1228009-94-6
• Molecular Weight: 531.571
• Mol File: 1228009-94-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[(4-benzoyl-5-phenyl-1-p-methoxyphenyl-1H-pyrazol-3-yl)carbonyl]-1-phenylsemicarbazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(4-benzoyl-5-phenyl-1-p-methoxyphenyl-1H-pyrazol-3-yl)carbonyl]-1-phenylsemicarbazide(1228009-94-6)
• EPA Substance Registry System: 1-[(4-benzoyl-5-phenyl-1-p-methoxyphenyl-1H-pyrazol-3-yl)carbonyl]-1-phenylsemicarbazide(1228009-94-6)

Safety Data

• Hazardous Substances Data: 1228009-94-6(Hazardous Substances Data)

Upstream product

• 1228009-90-2 4-benzoyl-5-phenyl-1-(4-methoxyphenyl)-1H-pyrazole-3-carbonyl chloride 
• 103-03-7 1-phenylsemicarbazide 

Relevant articles and documents

Synthesis and reactions of 4-benzoyl-1,5-diaryl-1h-pyrazole-3-carbonyl chlorides with various semi- and thiosemicarbazides

(Chemical Equation Presented) The 1H-pyrazole-3-carboxylic acids 2 were converted via reactions of their acid chlorides 3 with some semi- and thiosemicarbazide derivatives into the corresponding new phenylsemi- and thiosemicarbazides 4a-e, 6, 5-(pyrazol-3-yl)-4H-1,2,4-triazol-3-thiones 5a,b, and 2-(pyrazol-3-yl)-1,3,4-thiadiazol 7 derivatives, in good yields (45-97%, respectively). The reactions of 4a,c,e with Lawesson reagent lead to the products 6 and 7 formation. The structures of these newly synthesized compounds were determined. from the IR, 1H- and 13C-NMR spectroscopic data and elemental analyses.