180780-15-8

Basic information

• Product Name: (2-chloro-phenyl)-[1]naphthyl ketone
• Synonyms: (2-chloro-phenyl)-[1]naphthyl ketone
• CAS NO: 180780-15-8
• Molecular Weight: 266.727
• Mol File: 180780-15-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2-chloro-phenyl)-[1]naphthyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-chloro-phenyl)-[1]naphthyl ketone(180780-15-8)
• EPA Substance Registry System: (2-chloro-phenyl)-[1]naphthyl ketone(180780-15-8)

Safety Data

• Hazardous Substances Data: 180780-15-8(Hazardous Substances Data)

Upstream product

• 879-18-5 naphthalene-1-carbonic acid chloride 
• 860395-76-2 1-(1-(2-chlorophenyl)vinyl)naphthalene 
• 609-65-4 o-chlorobenzoyl chloride 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 860395-76-2 1-(1-(2-chlorophenyl)vinyl)naphthalene 
• 82-05-3 7H-benz[d,e]anthracene-7-one 

Relevant articles and documents

Photo-induced oxidative cleavage of C-C double bonds for the synthesis of biaryl methanoneviaCeCl3catalysis

A Ce-catalyzed strategy is developed to produce biaryl methanonesviaphotooxidative cleavage of C-C double bonds at room temperature. This reaction is performed under air and demonstrates high activity as well as functional group tolerance. A synergistic Ce/ROH catalytic mechanism is also proposed based on the experimental observations. This protocol should be the first successful Ce-catalyzed photooxidation reaction of olefins with air as the oxidant, which would provide inspiration for the development of novel Ce-catalyzed photochemical synthesis processes.

Ni and Cu-catalyzed one pot synthesis of unsymmetrical 1,3-di(hetero)aryl-1: H -indazoles from hydrazine, o -chloro (hetero)benzophenones, and (hetero)aryl bromides

The nickel-catalyzed cyclization of in situ generated ortho-chlorobenzophenone hydrazone derivatives, to afford 3-(hetero)aryl-1H-indazoles, is documented for the first time. The product 1H-indazoles can be transformed subsequently in a one-pot procedure into 1,3-di(hetero)aryl-1H-indazoles via copper-catalyzed N-arylation with (hetero)aryl bromides.