7504-29-2

Basic information

• Product Name: 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone
• CAS NO: 7504-29-2
• Molecular Formula: C₁₄H₁₀Cl₂O
• Molecular Weight: 265.1346
• Mol File: 7504-29-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 358.8°C at 760 mmHg
• Flash Point: 151.6°C
• Density: 1.289g/cm³
• Vapor Pressure: 2.49E-05mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone(7504-29-2)
• EPA Substance Registry System: 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone(7504-29-2)

Safety Data

• Hazardous Substances Data: 7504-29-2(Hazardous Substances Data)

Usage

General Description

1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is a chemical compound with the formula C14H9Cl2O. It is a ketone with two phenyl rings, one of which is substituted with a chlorine atom at the 2-position and the other with a chlorine atom at the 4-position. 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various pharmaceuticals and agrochemicals. It can also be used as a reagent in the preparation of other organic compounds. Its properties and structure make it an important intermediate in the production of a wide range of chemicals.

Upstream product

• 26037-50-3 tri(4-chloro)benzyl aluminium 
• 89-98-5 2-chloro-benzaldehyde 
• 609-65-4 o-chlorobenzoyl chloride 
• 622-95-7 4-chlorobenzyl bromide 
• 107323-82-0 4-chlorobenzylmagnesium bromide 
• 609-66-5 2-chlorobenzamide 
• 873-32-5 2-Chlorobenzonitrile 

Downstream Products

• 1153577-12-8 C₂₂H₁₇Cl₂N₃ 
• 1153577-11-7 C₁₈H₁₅Cl₂N₃ 
• 1153577-08-2 C₁₅H₁₁Cl₂N₃S 
• 736994-05-1 7-(2-chlorophenyl)-8-(4-chlorophenyl)-2-methylpyrazolo[1,5-a][1,3,5]triazin-4(3H)-one 
• 1067649-41-5 C₂₄H₂₃Cl₂N₇O 
• 1067649-06-2 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-N-isopropylpyrido[2,3-d]pyrimidin-4-amine 
• 1067649-05-1 N-[2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4-yl]methanesulfonamide 
• 1067649-58-4 2-amino-6-(2-chlorophenyl)-5-(4-chlorophenyl)nicotinamide 
• 1067649-57-3 2-amino-6-(2-chlorophenyl)-5-(4-chlorophenyl)nicotinonitrile 
• 1067649-55-1 ethyl 4-chloro-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-2-carboxylate 
• 1067649-54-0 methyl 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-4-carboxylate 
• 1067649-53-9 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-4-(4-fluorophenyl)pyrido[2,3-d]pyrimidine 
• 1067649-52-8 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-4-carbonitrile 
• 916728-81-9 2-bromo-1-(2-chlorophenyl)-2-(4-chlorophenyl)-ethanone 

Relevant articles and documents

Tandem nucleophilic addition-Oppenauer oxidation of aromatic aldehydes to aryl ketones with triorganoaluminium reagents

In the presence of pinacolone, the in situ prepared triorganoaluminium reagents reacted with aromatic aldehydes to give ketones in moderate to high yield. We propose that the products are formed via a tandem organoaluminium reagents addition-Oppenauer oxidation sequence. The Royal Society of Chemistry 2013.

PREPARATION OF 3-AMINO-4,5-DISUBSTITUTED-PYRAZOLE DERIVATIVES

A process for preparing a compound of Formula (I) is described herein as well as rocesses for using this compound to prepare other useful intermediates and compounds.