147801-94-3

Basic information

• Product Name: Ethanone, 1-[2-(4-methoxybenzoyl)phenyl]-
• CAS NO: 147801-94-3
• Molecular Formula: C16H14O3
• Molecular Weight: 254.285
• Mol File: 147801-94-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-(4-methoxybenzoyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-(4-methoxybenzoyl)phenyl]-(147801-94-3)
• EPA Substance Registry System: Ethanone, 1-[2-(4-methoxybenzoyl)phenyl]-(147801-94-3)

Safety Data

• Hazardous Substances Data: 147801-94-3(Hazardous Substances Data)

Upstream product

• 94-30-4 ethyl 4-methoxybenzoate 
• 100-09-4 4-methoxybenzoic acid 
• 1588511-52-7 (4-methoxyphenyl)(2-vinylphenyl)methanone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 1588511-50-5 C₁₇H₁₆N₂O₂S₂ 
• 1588511-51-6 N-methoxy-N-methyl-2-vinylbenzamide 
• 100961-61-3 2-[(benzo[d]thiazol-2-ylthio)methyl]benzoic acid 
• 7115-89-1 2-(bromomethyl)benzoic acid 
• 119290-28-7 o-hydroxyacetophenone 4-methoxybenzoyl hydrazone 
• 3290-99-1 4-methoxybenzoic acid hydrazide 
• 119290-28-7 4-Methoxy-benzoic acid [1-(2-hydroxy-phenyl)-eth-(E)-ylidene]-hydrazide 

Downstream Products

• 1588511-76-5 1-(4-methoxyphenyl)-4-methylphthalazine 

Relevant articles and documents

Iodine-promoted oxidative conversion of o-vinyl diaryl ketones into o-acetyl diaryl ketones, synthesis of 1-methyl-4-arylphthalazines as analogues of podophyllotoxin

A new method is described for the metal-free oxidation of o-vinyl diaryl ketones in the presence of molecular iodine or N-iodosuccinimide to give o-acetyl diaryl ketones. This transformation involves the initial formation of an iodohydrin, and the o-carbo

Regioselective quadruple domino aldolization/aldol condensation/Michael/ SNAr-cyclization: Construction of hexacyclic indeno-fused C-nor-D-homo-steroid frameworks

An operationally simple and highly atom-economic anionic quadruple domino reaction sequence for the synthesis of hexacyclic indeno-fused naphthalene/quinoline molecules having structural resemblance with the C-nor-D-homo-steroid nucleus has been developed. Promoter and solvent specificity, regioselectivity and mechanistic details were experimentally established. Catalyst concentration and solvent dependent switching of domino steps creating four new C-C bonds are discussed.

Synthesis of 1,2-diacylbenzenes from o-hydroxyaryl ketone acylhydrazones using [(diacetoxy)iodo]benzene

2'-Hydroxyacetophenone and 2'-hydroxypropiophenone acylhydrazones 3 are oxidized to 1,2-diacylbenzenes 4 using [(diacetoxy)iodo]benzene in dichloromethane at room temperature in a synthetically useful and high yield reaction.