74882-52-3

Basic information

• Product Name: 2-benzylidene-1-(2-methoxycarbonylphenyl)hydrazine
• Synonyms: 2-benzylidene-1-(2-methoxycarbonylphenyl)hydrazine
• CAS NO: 74882-52-3
• Molecular Weight: 254.288
• Mol File: 74882-52-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-benzylidene-1-(2-methoxycarbonylphenyl)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzylidene-1-(2-methoxycarbonylphenyl)hydrazine(74882-52-3)
• EPA Substance Registry System: 2-benzylidene-1-(2-methoxycarbonylphenyl)hydrazine(74882-52-3)

Safety Data

• Hazardous Substances Data: 74882-52-3(Hazardous Substances Data)

Upstream product

• 4036-59-3 2-benzylidene-1-(2-carboxyphenyl)hydrazine 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 52745-10-5 N-(phenylmethyl)-2-nitrobenzamide 
• 67-56-1 methanol 
• 150483-54-8 N-benzyl-2-nitrosobenzamide 
• 56070-95-2 3-benzylideneamino-1,2,3-benzotriazin-4-one 

Downstream Products

• 686268-74-6 methyl 2-[2-benzylidene-1-(3-ethoxy-3-oxopropanoyl)hydrazino]benzoate 
• 686268-75-7 ethyl 4-hydroxy-2-oxo-1-{[phenylmethylene]amino}-1,2-dihydroquinoline-3-carboxylate 

Relevant articles and documents

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The present invention provides HCV polymerase inhibiting compounds having the formula (I) where R1is cyclobutyl-N(Ra)-, n is 1, 2, 3 or 4, and at least one R5 is RaSO2N(Rj)alkyl-. In a non-

Electrosynthesis and in situ chemical rearrangement of o-nitrosobenzamides

Primary and secondary o-nitrosobenzamides can be prepared in a "redox" cell but are unstable in the solvent used for electrolysis (acetate buffer-alcohol).At room temperature N-aryl-2-nitrosobenzamides give 2-carboxyazobenzenes.N-alkyl-2-nitrosobenzamides decompose thermally into 2-methoxy or 2-ethoxycarbonylphenylhydrazones according to the alcohol used.Similarly, methyl benzoate (or ethyl benzoate) is obtained from 2-nitrosobenzamide.A possible mechanism involves an unstable heterocycle formed by the coupling of the two nitrogen atoms (nitroso and amide) followed by cleavage of the carbonyl-nitrogen bond resulting from nucleophilic attack of the solvent (water or alcohol). Key Words: flow cell electrosynthesis / 2-nitrosobenzamides / 2-carboxyazobenzenes / 2-alkoxycarbonylphenylhydrazones / indazol-3-one