58122-02-4

Basic information

• Product Name: 1-Propanone, 3-[4-(dimethylamino)phenyl]-1-phenyl-
• CAS NO: 58122-02-4
• Molecular Formula: C17H19NO
• Molecular Weight: 253.344
• Mol File: 58122-02-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-[4-(dimethylamino)phenyl]-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-[4-(dimethylamino)phenyl]-1-phenyl-(58122-02-4)
• EPA Substance Registry System: 1-Propanone, 3-[4-(dimethylamino)phenyl]-1-phenyl-(58122-02-4)

Safety Data

• Hazardous Substances Data: 58122-02-4(Hazardous Substances Data)

Upstream product

• 96-09-3 styrene oxide 
• 1703-46-4 N,N-dimethyl-4-hydroxymethylaniline 
• 1074-12-0 phenylglyoxal hydrate 
• 2039-80-7 N,N-dimethy-4-vinylaniline 
• 22965-98-6 4-(dimethylamino)chalcone 
• 98-86-2 acetophenone 
• 100-10-7 4-dimethylamino-benzaldehyde 
• 50-00-0 formaldehyd 
• 59276-79-8 3-(4-aminophenyl)-1-phenylpropan-1-one 
• 29546-14-3 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-N,N-dimethylaniline 
• 120-46-7 1,3-diphenylpropanedione 
• 1030-27-9 4-dimethylamino-chalcone 
• 98-85-1 1-Phenylethanol 

Downstream Products

• 2574-34-7 4-(1,3-diphenyl-4,5-dihydro-1H-pyrazol-5-yl)-N,N-dimethylaniline 
• 58122-05-7 N,N-dimethyl-4-((2-phenyl-1H-indol-3-yl)methyl)aniline 
• 61134-83-6 1-phenyl-3-(4'-dimethylaminophenyl)-1-propanol 

Relevant articles and documents

Synthesis of α-Alkylated Ketones via Selective Epoxide Opening/Alkylation Reactions with Primary Alcohols

A new method for converting terminal epoxides and primary alcohols into α-alkylated ketones under borrowing hydrogen conditions is reported. The procedure involves a one-pot epoxide ring opening and alkylation via primary alcohols in the presence of an N-heterocyclic carbene iridium(I) catalyst, under aerobic conditions, with water as the side product.

Visible-Light-Promoted Photocatalyst-Free Hydroacylation and Diacylation of Alkenes Tuned by NiCl2·DME

Herein, we describe a visible light-promoted hydroacylation strategy that facilitates the preparation of ketones from alkenes and 4-acyl-1,4-dihydropyridines via an acyl radical addition and hydrogen atom transfer pathway under photocatalyst-free conditions. The efficiency was highlighted by wide substrate scope, good to high yields, successful scale-up experiments, and expedient preparation of highly functionalized ketone derivatives. In addition, this protocol allows for the synthesis of 1,4-dicarbonyl compounds through alkene diacylation in the presence of NiCl2·DME.

Compounding method for beta-aryl propiophenone compound

The invention discloses a compounding method for a beta-aryl propiophenone compound. The compounding method is characterized by taking chalcone compounds as reaction substrates, and selectively chemically reducing the carbon-carbon double bonds in the rea