1259017-35-0

Basic information

• Product Name: 1-(phenylethynyl)-2-(1-phenylvinyl)benzene
• Synonyms: 1-(phenylethynyl)-2-(1-phenylvinyl)benzene
• CAS NO: 1259017-35-0
• Molecular Weight: 280.369
• Mol File: 1259017-35-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(phenylethynyl)-2-(1-phenylvinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(phenylethynyl)-2-(1-phenylvinyl)benzene(1259017-35-0)
• EPA Substance Registry System: 1-(phenylethynyl)-2-(1-phenylvinyl)benzene(1259017-35-0)

Safety Data

• Hazardous Substances Data: 1259017-35-0(Hazardous Substances Data)

Upstream product

• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 15912-74-0 triphenyl(methyl)phosphonium 
• 221458-86-2 (phenyl)[2-(2-phenylethynyl)phenyl]methanone 
• 24892-82-8 1-bromo-2-(1-phenylpropen-1-yl)benzene 
• 536-74-3 phenylacetylene 
• 591-50-4 iodobenzene 

Downstream Products

• 848-83-9 1,3-diphenylnaphthalene 
• 1259017-23-6 ethyl (E)-3-(2,4-diphenylnaphthalen-1-yl)acrylate 
• 796-30-5 1,4-diphenylnaphthalene 

Relevant articles and documents

Palladium-Catalyzed Aerobic Oxidative Coupling of ortho-(Alkynyl)styrenes with Allylic Alcohols via 6- endo-dig Cyclization: Regioselective Construction of Polysubstituted Naphthalenes

An efficient protocol is described for the regioselective construction of polysubstituted functionalized naphthalenes from easily accessible ortho-(alkynyl)styrenes under mild reaction conditions. The reaction proceeds via cycloaromatization and intermole

Gold versus palladium: A regioselective cycloisomerization of aromatic enynes

Aromatic enynes can be transformed into arylnaphthalenes or benzofulvenes depending on the reaction conditions. Under gold(I) catalysis, exclusive or major 6-endo-dig cyclization took place leading to arylnaphthalenes. However, a catalytic system based on