943913-77-7

Basic information

• Product Name: 1-acetyl-N-(4-methoxyphenyl)cyclopropanecarboxamide
• Synonyms: 1-acetyl-N-(4-methoxyphenyl)cyclopropanecarboxamide
• CAS NO: 943913-77-7
• Molecular Weight: 233.267
• Mol File: 943913-77-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-acetyl-N-(4-methoxyphenyl)cyclopropanecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-acetyl-N-(4-methoxyphenyl)cyclopropanecarboxamide(943913-77-7)
• EPA Substance Registry System: 1-acetyl-N-(4-methoxyphenyl)cyclopropanecarboxamide(943913-77-7)

Safety Data

• Hazardous Substances Data: 943913-77-7(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 1220042-26-1 C₁₆H₁₇NO₃ 
• 5437-98-9 4'-methoxyacetoacetanilide 
• 106-93-4 ethylene dibromide 

Downstream Products

• 1021876-11-8 1-(1-(hydroxyimino)ethyl)-N-(4-methoxyphenyl)cyclopropanecarboxamide 
• 1173161-11-9 C₂₁H₂₁NO₃ 
• 1220042-26-1 C₁₆H₁₇NO₃ 
• 1326775-70-5 5-(4-methoxyphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one 
• 1381883-65-3 3,3'-(5-(4-methoxyphenyl)-4-oxo-6-(p-tolyl)-2,3,4,5,6,7-hexahydrofuro[3,2-c]pyridine-7,7-diyl)dipropanenitrile 
• 1373611-05-2 N-(4-methoxyphenyl)cyclopropane-1,1-dicarboxamide 
• 1373611-15-4 methyl 1-[(4-methoxyphenyl)carbamoyl]cyclopropane-1-carboxylate 
• 1353889-56-1 5-(4-methoxyphenyl)-6-methyl-5-azaspiro[2.3]hexan-4-one 
• 1259291-12-7 7-benzylidene-5-(4-methoxyphenyl)-6-phenyl-5-azaspiro[2.5]octane-4,8-dione 

Relevant articles and documents

Copper(I)-Catalyzed Intramolecular N-N Coupling of Cyclopropyl O-Acyl Ketoximes: Synthesis of Spiro-fused Pyrazolin-5-ones

A convenient copper-catalyzed approach has been developed for the synthesis of substituted spiro-fused pyrazolin-5-ones from readily available cyclopropyl O-acyl ketoximes via an intramolecular N N bond formation reaction. These catalytic reactions proceed in excellent yields with a broad scope.

Ag-containing all-carbon 1,3-dipoles: Generation and formal cycloaddition for furo[3,2-b]-β/γ-lactams

A new strategy for highly diastereoselective synthesis of furo[3,2-b]-β-lactams and furo[3,2-b]-γ-lactams via a novel Ag(i)-mediated intramolecular 1,3-dipolar cycloaddition of oxo-N- propargylamides, is developed and the possible mechanism of these trans