49747-52-6

Basic information

• Product Name: 1-(3,4-dimethoxyphenyl)-3-phenylpropan-1-one
• Synonyms: 1-(3,4-dimethoxyphenyl)-3-phenylpropan-1-one
• CAS NO: 49747-52-6
• Molecular Weight: 270.328
• Mol File: 49747-52-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dimethoxyphenyl)-3-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxyphenyl)-3-phenylpropan-1-one(49747-52-6)
• EPA Substance Registry System: 1-(3,4-dimethoxyphenyl)-3-phenylpropan-1-one(49747-52-6)

Safety Data

• Hazardous Substances Data: 49747-52-6(Hazardous Substances Data)

Upstream product

• 53744-27-7 3,4-dimethoxychalcone 
• 108-86-1 bromobenzene 
• 82588-90-7 Methyl 3-(3,4-dimethoxyphenyl)-3-hydroxy-2-methylenepropanoate 
• 100-51-6 benzyl alcohol 
• 183303-74-4 1-(3,4-dimethoxyphenyl)-2-phenoxy-1-ethanol 
• 91-16-7 1,2-dimethoxybenzene 
• 151647-54-0 3-phenyl-1-pyrrolidin-1-yl-propane-1-one 
• 536-74-3 phenylacetylene 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 4087-66-5 (E)-3-(2-bromophenyl)-1-(3,4-dimethoxyphenyl)prop-2-en-1-one 
• 4087-66-5 1-(3,4-dimethoxyphenyl)-3-phenylprop-2-en-1-one 
• 591-50-4 iodobenzene 
• 31706-95-3 1'-Hydroxymethyleugenol 

Downstream Products

• 49747-68-4 4-(1-chloro-3-phenyl-propyl)-1,2-dimethoxy-benzene 
• 49747-80-0 4-[1-(3,4-dimethoxy-phenyl)-3-phenyl-propyl]-morpholine 
• 49747-67-3 1-(3,4-Dimethoxy-phenyl)-3-phenyl-propan-1-ol 
• 101878-37-9 1-(3,4-dimethoxy-phenyl)-3-phenyl-propane-1,2-dione-2-oxime 
• 52947-25-8 2-amino-1-(3,4-dimethoxy-phenyl)-3-phenyl-propan-1-ol 

Relevant articles and documents

Direct conversion of secondary propargyl alcohols into 1,3-di-arylpropanoneviaDBU promoted redox isomerization and palladium assisted chemoselective hydrogenation in a single pot operation

Palladium(ii)acetate is found to be an efficient catalyst for the single-step conversion of secondary propargyl alcohols to 1,3-diarylpropanone derivatives under mild basic conditions. The reaction is believed to proceedviaredox isomerisation of secondary propargyl alcohols followed by chemoselective reduction of an enone double bond with formic acid as an adequate hydrogen donor. A large number of 1,3-diarylpropanone derivatives may readily be prepared from a milligram to a multigram scale.

New Friedel-Crafts strategy for preparing 3-acylindoles

A selective Friedel-Crafts acylation of indoles via an unusual cleavage of the amide C-N bond was achieved by triflic anhydride activation. This method offers rapid efficient access to high-biological-value 3-acylindoles, performs a series of scrupulous mechanistic studies and offers a strong courage that amide synthons can form new C-C bonds under transition-metal-free conditions.

[Pd]-Catalyzed Intermolecular Coupling and Acid Mediated Intramolecular Cyclodehydration: One-Pot Synthesis of Indenes

An efficient one-pot synthesis of indenes from simple starting materials is presented. This process involves a dual C–C bond formation through an intermolecular Heck coupling reaction followed by acid-mediated intramolecular cyclodehydration. The strategy