93534-17-9

Basic information

• Product Name: 2-(2,4-dichlorophenyl)-1-phenylethanone
• Synonyms: 2-(2,4-dichlorophenyl)-1-phenylethanone
• CAS NO: 93534-17-9
• Molecular Weight: 265.139
• Mol File: 93534-17-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(2,4-dichlorophenyl)-1-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-dichlorophenyl)-1-phenylethanone(93534-17-9)
• EPA Substance Registry System: 2-(2,4-dichlorophenyl)-1-phenylethanone(93534-17-9)

Safety Data

• Hazardous Substances Data: 93534-17-9(Hazardous Substances Data)

Usage

Physical state

Yellow solid

Odor

Distinct

Usage in synthesis

Pharmaceutical and organic compounds

Intermediate in production

Pesticides and agrochemicals

Industrial applications

Perfumes and flavorings

Investigated properties

Antitumor and antibacterial

Upstream product

• 369-57-3 benzenediazonium tetrafluoroborate 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 100-42-5 styrene 
• 13123-92-7 (2,4-dichlorophenyl)hydrazine 
• 603-33-8 triphenylbismuthane 
• 53056-20-5 2,4-dichlorophenylacetyl chloride 

Downstream Products

• 1566598-76-2 ethyl 4-(2,4-dichlorophenyl)-1,5-diphenyl-1H-pyrazole-3-carboxylate 
• 1566598-91-1 ethyl 4-(2,4-dichlorophenyl)-5-phenyl-1-(2,4,6-trichlorophenyl)-1H-pyrazole-3-carboxylate 
• 96223-58-4 1-[(4S,5R)-4-(2,4-Dichloro-phenyl)-2-oxo-5-phenyl-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 96223-58-4 1-[(4S,5S)-4-(2,4-Dichloro-phenyl)-2-oxo-5-phenyl-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 107710-88-3 (2R,3S)-2-(2,4-Dichloro-phenyl)-3-phenyl-1-[1,2,4]triazol-1-yl-butane-2,3-diol 
• 107680-04-6 (2R,3R)-2-(2,4-Dichloro-phenyl)-3-phenyl-1-[1,2,4]triazol-1-yl-butane-2,3-diol 
• 107680-31-9 (2S,3R)-1-(4-Chloro-phenyl)-3-(2,4-dichloro-phenyl)-2-phenyl-4-[1,2,4]triazol-1-yl-butane-2,3-diol 
• 107680-23-9 (2R,3S)-2-(2,4-Dichloro-phenyl)-3-phenyl-1-[1,2,4]triazol-1-yl-heptane-2,3-diol 
• 107659-70-1 (4S,5R)-4-(2,4-Dichloro-phenyl)-5-phenyl-4-[1,2,4]triazol-1-ylmethyl-[1,3]dioxolan-2-one 
• 107679-95-8 (4S,5R)-4-(2,4-Dichloro-phenyl)-4-imidazol-1-ylmethyl-5-phenyl-[1,3]dioxolan-2-one 
• 107659-87-0 1-[(4R,5S)-4-(2,4-Dichloro-phenyl)-5-phenyl-[1,3]dioxolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 96223-35-7 (1R,2S)-2-(2,4-Dichloro-phenyl)-1-phenyl-3-[1,2,4]triazol-1-yl-propane-1,2-diol 
• 94147-49-6 2-(2,4-Dichloro-phenyl)-2-hydroxy-1-phenyl-3-[1,2,4]triazol-1-yl-propan-1-one 
• 96223-53-9 (1R,2S)-2-(2,4-Dichloro-phenyl)-3-imidazol-1-yl-1-phenyl-propane-1,2-diol 

Relevant articles and documents

Palladium-catalyzed synthesis of α-aryl acetophenones from styryl ethers and aryl diazonium saltsviaregioselective Heck arylation at room temperature

Preparation of α-aryl acetophenones from styryl ethers and aryldiazonium salts is described. The reaction is catalyzed by palladium acetate at room temperature in the absence of ligand and base. The developed method is highly attractive in terms of reaction conditions, substrate scope, functional group tolerance and yields. Synthetic applications of the present method are demonstrated by preparing α-aryl indoles and 3-aryl isocoumarin from styryl ethers.

Pd-catalyzed synthesis of α-aryl ketones through couplings of α-arylacetyl chlorides with triarylbismuths as multi-coupling nucleophiles

The cross-coupling reaction of α-arylacetyl chlorides with triarylbismuths was studied under Pd-catalyzed conditions. The reaction was found to be facile under the established protocol and furnished high yields of α-aryl ketones in short reaction times. T