65622-34-6

Basic information

• Product Name: 2-Propanone, 1,3-bis(4-chlorophenyl)-
• CAS NO: 65622-34-6
• Molecular Formula: C15H12Cl2O
• Molecular Weight: 279.166
• Mol File: 65622-34-6.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: 2-Propanone, 1,3-bis(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanone, 1,3-bis(4-chlorophenyl)-(65622-34-6)
• EPA Substance Registry System: 2-Propanone, 1,3-bis(4-chlorophenyl)-(65622-34-6)

Safety Data

• Hazardous Substances Data: 65622-34-6(Hazardous Substances Data)

Upstream product

• 1878-66-6 4-chlorophenylacetic Acid 
• 14062-24-9 4-chloro-benzeneacetic acid, ethyl ester 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 4755-77-5 Ethyl oxalyl chloride 
• 622-95-7 4-chlorobenzyl bromide 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 1387574-29-9 1-(4-chlorophenyl)-3-(4-cyanophenyl)propane-2-one 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 109812-84-2 1,5-bis-(4-chloro-phenyl)-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 38268-10-9 tetrakis-(4-chloro-phenyl)-cyclopentadienone 
• 38268-04-1 2,5-bis(4-chlorophenyl)-3,4-diphenylcyclopenta-2,4-dienone 
• 23923-19-5 4-Phenyl-2,3,5-tris-(p-chlor-phenyl)-(αα'β)-cyclopentadien-(2,4)-on-(1) 
• 3327-51-3 4-chlorobenzyl radical 
• 501034-26-0 1,3-dibromo-1,3-bis-(4-chloro-phenyl)-propan-2-one 
• 133707-66-1 4,6-bis-(4-chloro-phenyl)-2-oxo-1,2-dihydro-pyridine-3-carbonitrile 

Relevant articles and documents

Fully Substituted Conjugate Benzofuran Core: Multiyne Cascade Coupling and Oxidation of Cyclopropenone

An unprecedented C═C double bond cleavage of cyclopropenone and dioxygen activation by multiyne cascade coupling has been developed. This chemistry provides a novel, simple, and efficient approach to synthesize fully substituted conjugate benzofuran derivatives from simple substrates under mild conditions. The density functional theory (DFT) calculations reveal that the unique homolytic cleavages of cyclopropenone and molecular oxygen are crucial to the success of this reaction.

Catalytic Asymmetric (3 + 3) Cycloaddition of Oxyallyl Zwitterions with α-Diazomethylphosphonates

The unique structure of oxyallyls represents a significant challenge for their catalytic asymmetric applications. Herein, an unprecedented chiral imidodiphosphoric acid-catalytic enantioselective (3 + 3) cycloaddition between oxyallyl zwitterions generate

Rh(III)-Catalyzed [3 + 3] Annulation Reaction of Cyclopropenones and Sulfoxonium Ylides toward Trisubstituted 2-Pyrones

A new Rh(III)-catalyzed [3 + 3] annulation reaction between cyclopropenones and β-ketosulfoxonium ylides has been reported, enabling metal carbene insertion to access a wide range of trisubstituted 2-pyrones with moderate to excellent yields via C-C single-bond cleavage, in which sulfoxonium ylides serve as potential safe precursors of metal carbenes. This reaction occurred under redox-neutral conditions with a broad substrate scope.