94418-01-6

Basic information

• Product Name: 3-Penten-2-one, 4-[(3-chlorophenyl)amino]-
• Synonyms: 4-(3-Chlor-anilino)-pent-3-en-2-on;4-(3-chloro-anilino)-pent-3-en-2-one;Acetylaceton-mono-(3-chlor-anil);3-Penten-2-one,4-[(3-chlorophenyl)amino];4-(3-chlorophenylamino)-3-penten-2-one
• CAS NO: 94418-01-6
• Molecular Formula: C11H12ClNO
• Molecular Weight: 209.675
• Mol File: 94418-01-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Penten-2-one, 4-[(3-chlorophenyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Penten-2-one, 4-[(3-chlorophenyl)amino]-(94418-01-6)
• EPA Substance Registry System: 3-Penten-2-one, 4-[(3-chlorophenyl)amino]-(94418-01-6)

Safety Data

• Hazardous Substances Data: 94418-01-6(Hazardous Substances Data)

Upstream product

• 108-42-9 3-chloro-aniline 
• 123-54-6 acetylacetone 

Downstream Products

• 1334474-15-5 3-acetyl-1-(3-chlorophenyl)-2-methyl-4-oxa-1-azacyclopenta[a]naphthalen-5-one 
• 88499-96-1 7-chloro-2,4-dimethyl-quinoline 

Relevant articles and documents

REACTIONS OF 4-AMINO-3-PENTEN-2-ONE AND ITS N-SUBSTITUTED REDIVATIVES WITH DIAZONIUM IONS

Azo coupling reactions of benzenediazonium salts with substituted 4-amino-3-penten-2-ones take place at the C-3 atom. 1H and 13C NMR spectroscopy has been used to study the structure of both the starting enaminones and coupling products.In CDCl3, 3-(4-chl

K-10 clay as a reusable catalyst for the solvent-free, MW-induced synthesis of enaminones

A series of β-amino-a,β-unsaturated ketones and esters were synthesized in good to excellent yields from the reaction of different amines with 1,3-dicarbonyl compounds in solvent-free media using montmorillonite K-10 clay as.

B2O3/Al2O3 as a new, highly efficient and reusable heterogeneous catalyst for the selective synthesis of β-enamino ketones and esters under solvent-free conditions

Boron oxide adsorbed on alumina (B2O3/Al 2O3) has been found to be a new and highly efficient heterogeneous catalyst for the synthesis of β-enamino ketones and esters by the enamination of various primary and secondary amines with β-dicarbonyl compounds under solvent-free conditions. The important features of this methodology are broad substrate scope, high yield, no requirement of metal catalysts, high regio-and chemoselectivity and environmental friendliness. In addition, the catalyst could be recovered easily after the reactions and reused without evident loss of reactivity.