126866-18-0

Basic information

• Product Name: 1-Propanone, 2-(4-chlorophenyl)-1-phenyl-
• CAS NO: 126866-18-0
• Molecular Formula: C15H13ClO
• Molecular Weight: 244.721
• Mol File: 126866-18-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 2-(4-chlorophenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 2-(4-chlorophenyl)-1-phenyl-(126866-18-0)
• EPA Substance Registry System: 1-Propanone, 2-(4-chlorophenyl)-1-phenyl-(126866-18-0)

Safety Data

• Hazardous Substances Data: 126866-18-0(Hazardous Substances Data)

Usage

Chemical class

Ketone

Usage

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds; reagent in organic reactions; building block in the preparation of various compounds

Additional applications

Forensic science, production of chemical weapons (e.g. tear gas)

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 99-91-2 para-chloroacetophenone 
• 191725-56-1 1-chloro-4-(1-methoxyprop-1-en-2-yl)benzene 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 5440-69-7 N-isopropylbenzamide 
• 637-87-6 1-Chloro-4-iodobenzene 
• 93-55-0 1-phenyl-propan-1-one 
• 673-32-5 1-Phenylprop-1-yne 
• 1073-67-2 4-vinylbenzyl chloride 
• 93-97-0 benzoic acid anhydride 
• 106-39-8 bromochlorobenzene 
• 304477-64-3 1-chloro-4-(1-phenylprop-1-enyl)benzene 
• 74-88-4 methyl iodide 

Downstream Products

• 2236-17-1 2-(4-Chloro-phenyl)-1-[4-(2-diethylamino-ethoxy)-phenyl]-1-phenyl-propan-1-ol 
• 2137-73-7 (2-{4-[(E)-2-(4-Chloro-phenyl)-1-phenyl-propenyl]-phenoxy}-ethyl)-diethyl-amine 

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.

Cross-Coupling of Secondary Amides with Tertiary Amides: The Use of Tertiary Amides as Surrogates of Alkyl Carbanions for Ketone Synthesis

In recent years, exciting progress has been made in the field of direct transformation of amides, nevertheless, the condensation between two amides remains rare and restricted to homo-coupling reactions. Herein, we report the cross-coupling of secondary amides with tertiary amides, which provides a synthesis of ketones under mild conditions, and features the use of tertiary amides as surrogates of alkyl carbanions. The method relies on the coupling of enamines, generated from tertiary amides by catalytic partial reduction of tertiary amides with Vaska's catalyst, with nitrilium ions, formed in situ from secondary amides via activation with trifluoromethanesulfonic anhydride, and on the subsequent deformylation.

From acetone metalation to the catalytic α-arylation of acyclic ketones with NHC-nickel(II) complexes

Air-stable N-heterocyclic carbene-nickel(II) complexes at concentrations as low as 1 mol% exhibit high catalytic activity for the α-arylation of acyclic ketones and join a highly restricted list of nickel catalysts for this key reaction. Mechanistic investigations suggest a radical pathway. the Partner Organisations 2014.