1591-44-2

Basic information

• Product Name: (4-chlorophenyl)(naphthalen-1-yl)methanone
• Synonyms: (4-chlorophenyl)(naphthalen-1-yl)methanone
• CAS NO: 1591-44-2
• Molecular Weight: 266.727
• Mol File: 1591-44-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4-chlorophenyl)(naphthalen-1-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chlorophenyl)(naphthalen-1-yl)methanone(1591-44-2)
• EPA Substance Registry System: (4-chlorophenyl)(naphthalen-1-yl)methanone(1591-44-2)

Safety Data

• Hazardous Substances Data: 1591-44-2(Hazardous Substances Data)

Upstream product

• 91-20-3 naphthalene 
• 122-01-0 4-chloro-benzoyl chloride 
• 13922-41-3 1-Naphthylboronic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 1251832-81-1 2-[(4-chlorophenyl)ethynyl]benzaldehyde 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 873-73-4 4-n-chlorophenylacetylene 
• 201230-82-2 carbon monoxide 
• 90-14-2 1-Iodonaphthalene 
• 17151-48-3 tributyl(4-chlorophenyl)stannane 
• 1679-18-1 4-Chlorophenylboronic acid 
• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 86-53-3 1-Cyanonaphthalene 

Downstream Products

• 147022-22-8 4-chlorophenyl-1-naphthylmethanol 
• 1591-43-1 1-(4-chlorobenzyl)naphthalene 
• 1591-41-9 4-(1-Naphthylmethyl)-benzhydrol 
• 1591-47-5 4-(1-Naphthylmethyl)-benzophenon 
• 147022-04-6 1-[(4-Chloro-phenyl)-naphthalen-1-yl-methyl]-1H-imidazole 

Relevant articles and documents

Carbomylative Suzuki-Miyaura coupling of arylboronic acids with aryl iodides catalyzed by the MCM-41-supported bidentate phosphane palladium(II) complex

The first heterogeneous carbonylative Suzuki-Miyaura cross-coupling reaction of arylboronic acids with aryl iodides under an atmospheric pressure of carbon monoxide has been achieved in anisole at, 80 °C in the presence of a catalytic amount of an MCM-41-supported bidentate phosphane palladium(II) complex (MCM-41-2P-PdII), yielding unsymmetrical biaryl ketones in good-to-high yields. This polymeric palladium catalyst exhibited higher activity and selectivity than fPdCl2(PPh3)2] and can be reused at least 10 times without any decrease in activity. Wiley-VCH Verlag GmbH & Co, KGaA.

Gold-catalyzed reactions of enynals/enynones with norbornenes: Generation and trapping of cyclic o-quinodimethanes (o-QDMs)

Fan-like structures: An efficient AuIII-catalyzed method to generate the highly reactive cyclic o-quinodimethane (o-QDM) species from easily available enynals or enynones is presented (see scheme). This method produced a variety of structurally unique fan-like products with the advantages of mild reaction conditions, excellent diastereoselectivities, and high functional-group tolerance. Copyright