159211-70-8

Basic information

• Product Name: 7-oxo-7-phenyldinaphtho<2,1-b;1',2'-d>phosphole
• CAS NO: 159211-70-8
• Molecular Weight: 376.394
• Mol File: 159211-70-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 7-oxo-7-phenyldinaphtho<2,1-b;1',2'-d>phosphole(CAS DataBase Reference)
• NIST Chemistry Reference: 7-oxo-7-phenyldinaphtho<2,1-b;1',2'-d>phosphole(159211-70-8)
• EPA Substance Registry System: 7-oxo-7-phenyldinaphtho<2,1-b;1',2'-d>phosphole(159211-70-8)

Safety Data

• Hazardous Substances Data: 159211-70-8(Hazardous Substances Data)

Upstream product

• 74866-28-7 2,2'-dibromo-1,1'-binaphthyl 
• 644-97-3 Dichlorophenylphosphine 
• 76144-87-1 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl 
• 5405-96-9 3,3',4,4'-tetrahydro-1,1'-binaphthalene 
• 149639-52-1 (+/-)-7-phenyldinaphtho<2,1-b;1',2'-d>phosphole 

Relevant articles and documents

New Access to Six-Membered Phosphacycle Annulated Polyaromatic Ring System

A facile Ag-catalyzed intramolecular C–P bond formation reaction from easily accessible phosphine oxides has been developed. Several new heteroatoms fused π-conjugated molecules were synthesized from this procedure with their structures confirmed by X-ray

Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two Carbon-Phosphorus Bonds by Nickel Catalysis

The nickel-catalyzed cyclization of bisphosphine derivatives to form various phosphacycles is reported. The reaction proceeds via the cleavage of two carbon-phosphorus bonds of the bisphosphine. Unlike the previously reported palladium catalysts, the use

Synthesis, crystal structure, dynamic behavior and reactivity of dinaphtho[2,1-b:1',2'-d]phospholes and related atropisomeric phosphacyclic derivatives

7-Phenyldinaphtho[2,1-b:1',2'-d]phosphole (1b) has been prepared by reaction of dichlorophenylphosphine either with 2,2'-dilithio-1,1'-binaphthalene or with bis-dialin 7. In the latter case the relevant tetrahydro derivative 8 is formed at the same time.