78002-37-6

Basic information

• Product Name: Hydrazinecarboxamide, 2-(1-methylethylidene)-N-phenyl-
• CAS NO: 78002-37-6
• Molecular Formula: C10H13N3O
• Molecular Weight: 191.233
• Mol File: 78002-37-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Hydrazinecarboxamide, 2-(1-methylethylidene)-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxamide, 2-(1-methylethylidene)-N-phenyl-(78002-37-6)
• EPA Substance Registry System: Hydrazinecarboxamide, 2-(1-methylethylidene)-N-phenyl-(78002-37-6)

Safety Data

• Hazardous Substances Data: 78002-37-6(Hazardous Substances Data)

Upstream product

• 5441-14-5 4-phenylsemicarbazide hydrochloride 
• 67-64-1 acetone 
• 127-09-3 sodium acetate 
• 62-53-3 aniline 
• 110-20-3 acetone semicarbazone 
• 537-47-3 4-phenyl-semicarbazide 

Downstream Products

• 2603-10-3 N-phenyl methyl carbamate 
• 22454-63-3 4'-Chloracetophenon-(4-phenylsemicarbazon) 
• 22454-68-8 2-(1-(4-methoxyphenyl)ethylidene)-N-phenylhydrazine-1-carboxamide 
• 22454-60-0 4'-Methylacetophenon-(4-phenylsemicarbazon) 
• 293325-99-2 C₁₅H₂₃N₃O 
• 1430321-33-7 C₁₄H₂₁N₃O 
• 537-47-3 4-phenyl-semicarbazide 
• 677733-44-7 C₁₇H₂₅N₃O 
• 24060-13-7 2-cyclohexylidene-N-phenylhydrazine-1-carboxamide 
• 21367-49-7 4,4'-dichloro-benzophenone 4-phenyl-semicarbazone 
• 21367-50-0 4,4'-dimethoxy-benzophenone 4-phenyl-semicarbazone 
• 21367-48-6 4,4'-dimethyl-benzophenone 4-phenyl-semicarbazone 
• 3043-79-6 2-(diphenylmethylene)-N-phenylhydrazinecarboxamide 
• 302604-58-6 C₁₃H₁₃N₃O₂ 

Relevant articles and documents

Synthesis and spectral characterization of zinc(II) and cadmium(II) complexes of acetone-N(4)-phenylsemicarbazone: Crystal structures of acetone-N(4)-phenylsemicarbazone and a cadmium(II) complex

Seven Zn(II) and Cd(II) complexes of ON donor acetone-N(4)- phenylsemicarbazone (HL) have been synthesized and physico-chemically characterized by partial elemental analyses, molar conductance measurements, infrared, electronic and 1H NMR spect

Anodic cleavage of several ketone N-phenylsemicarbazones into methyl N-phenylcarbamate and the corresponding dimethyl acetals

Several ketone N-phenylsemicarbazones were electrooxidized in the presence of potassium iodide and a base using methanol as the solvent to give nearly commensurate amounts of methyl N-phenylcarbamate and the corresponding dimethyl acetals. Continuous evolution of gaseous nitrogen was observed from the anolyte during the electrooxidation. The reactions were carried out under very mild reaction conditions and are presumed to proceed through a four-electron oxidation process, in which the iodide ion plays an important role as an electron carrier.