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

Description

1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is a chemical compound with the formula C14H9Cl2O. It is a ketone featuring two phenyl rings, one substituted with a chlorine atom at the 2-position and the other at the 4-position. 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is significant in the field of organic synthesis and pharmaceutical research.

Uses

Used in Pharmaceutical Research:
1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable intermediate in the development of a wide range of medicinal compounds.
Used in Agrochemicals:
In the agrochemical industry, 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is utilized as a key component in the creation of different agrochemicals, contributing to its importance in this sector.
Used in Organic Synthesis:
As a reagent, 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone is employed in the preparation of other organic compounds, highlighting its versatility and applicability in organic chemistry.
Used in Chemical Production:
1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone serves as an important intermediate in the production of a broad spectrum of chemicals, underlining its significance in the chemical industry.

Upstream product

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

Downstream Products

• 654668-43-6 1-(2-chlorophenyl)-2-(4-chlorophenyl)-3-(dimethylamino)prop-2-en-1-one 
• 916728-81-9 2-bromo-1-(2-chlorophenyl)-2-(4-chlorophenyl)-ethanone 
• 611220-83-8 6-(2-chlorophenyl)-5-(4-chlorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile 
• 611220-89-4 2-chloro-6-(2-chlorophenyl)-5-(4-chlorophenyl)-pyridine-3-carbonitrile 
• 1065267-58-4 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4-amine 
• 1065267-60-8 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one 
• 1065267-61-9 2-tert-butyl-4-chloro-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine 
• 1065267-63-1 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-4-hydrazinopyrido[2,3-d]pyrimidine 
• 1065266-53-6 5-tert-butyl-8-(2-chlorophenyl)-9-(4-chlorophenyl)pyrido[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine 
• 1067649-52-8 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-4-carbonitrile 
• 1067649-53-9 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-4-(4-fluorophenyl)pyrido[2,3-d]pyrimidine 
• 1067649-54-0 methyl 2-tert-butyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-4-carboxylate 
• 1067649-55-1 ethyl 4-chloro-7-(2-chlorophenyl)-6-(4-chlorophenyl)pyrido[2,3-d]pyrimidine-2-carboxylate 
• 1067649-57-3 2-amino-6-(2-chlorophenyl)-5-(4-chlorophenyl)nicotinonitrile 

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.