1450812-53-9

Basic information

• Product Name: N'-(4-methoxyphenyl)-N'-methylacetohydrazide
• Synonyms: N'-(4-methoxyphenyl)-N'-methylacetohydrazide
• CAS NO: 1450812-53-9
• Molecular Weight: 194.233
• Mol File: 1450812-53-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N'-(4-methoxyphenyl)-N'-methylacetohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(4-methoxyphenyl)-N'-methylacetohydrazide(1450812-53-9)
• EPA Substance Registry System: N'-(4-methoxyphenyl)-N'-methylacetohydrazide(1450812-53-9)

Safety Data

• Hazardous Substances Data: 1450812-53-9(Hazardous Substances Data)

Upstream product

• 17473-78-8 N’-(4-methoxyphenyl)acetohydrazide 
• 74-88-4 methyl iodide 
• 3471-32-7 4-Methoxyphenylhydrazine 

Downstream Products

• 412284-09-4 3-ethyl-1,2-dimethyl-5-methoxyindole 
• 2731-01-3 (±)-5-methoxy-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo-[2,3-b]indole 

Relevant articles and documents

Rh(III)-catalyzed oxidative coupling of 1,2-disubstituted arylhydrazines and olefins: A new strategy for 2,3-dihydro-1H-indazoles

A rhodium(III)-catalyzed oxidative olefination of 1,2-disubstituted arylhydrazines with alkenes via sp2 C-H bond activation followed by an intramolecular aza-Michael reaction is described. This strategy allows the direct and efficient construct

Formation of enehydrazine intermediates through coupling of phenylhydrazines with vinyl halides: Entry into the Fischer indole synthesis

Cut to the chase: Direct formation of an enehydrazine, an intermediate in the classic Fischer indole synthesis, solves the regioselectivity problem associated with indolization. This approach not only achieves selective synthesis of indoles through proper selection of the vinyl halide, but also leads to quick construction of desoxyeseroline and esermethole, as well as the key structural motif in the Akuammiline alkaloid vincorine. Copyright