1172591-90-0

Basic information

• Product Name: 1-benzyl-2-(phenylethynyl)benzene
• Synonyms: 1-benzyl-2-(phenylethynyl)benzene
• CAS NO: 1172591-90-0
• Molecular Weight: 268.358
• Mol File: 1172591-90-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-benzyl-2-(phenylethynyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-2-(phenylethynyl)benzene(1172591-90-0)
• EPA Substance Registry System: 1-benzyl-2-(phenylethynyl)benzene(1172591-90-0)

Safety Data

• Hazardous Substances Data: 1172591-90-0(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 583-55-1 1-Bromo-2-iodobenzene 
• 21375-88-2 1-bromo-2-(phenylethenyl)benzene 
• 100-39-0 benzyl bromide 
• 28059-64-5 2-benzylaniline 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 
• 529-23-7 o-aminobenzaldehyde 
• 35444-93-0 ortho-benzyliodobenzene 
• 100-58-3 phenylmagnesium bromide 
• 221458-84-0 [2-(hydroxyphenylmethyl)phenyl]phenylacetylene 
• 100-52-7 benzaldehyde 

Downstream Products

• 1418135-89-3 3-(4-nitrophenyl)-1,2-diphenyl-1H-indene 
• 1498-71-1 9-benzylanthracene 
• 5324-00-5 2,3-diphenyl-1H-indene 
• 1359715-97-1 1-benzyl-3,4-diphenylisoquinoline 
• 18636-54-9 1,2-diphenyl-1H-indene 

Relevant articles and documents

Synthesis of Cycloheptatrienes, Oxepines, Thiepines, and Silepines: A Comparison between Br?nsted Acid and Au-Catalysis

The cyclization of 1-(benzyl-, oxyaryl-, thioaryl-, and silaaryl)-2-ethynylbenzenes under Br?nsted acid- and Au(I)-catalysis is described. Br?nsted acid catalysis favors without exception the formation of the products derived from the regioselective proto

Synthesis of functionalized 1 H -indenes via copper-catalyzed arylative cyclization of arylalkynes with aromatic sulfonyl chlorides

A variety of polysubstituted 1H-indenes can be prepared through the copper-catalyzed arylative cyclization of simple arylalkynes with commercially available aromatic sulfonyl chlorides that function as an aryl group donor. The reaction tolerates a broad r