1265154-01-5

Basic information

• Product Name: (Z)-4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl acetate
• Synonyms: (Z)-4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl acetate
• CAS NO: 1265154-01-5
• Molecular Weight: 276.335
• Mol File: 1265154-01-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (Z)-4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl acetate(1265154-01-5)
• EPA Substance Registry System: (Z)-4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl acetate(1265154-01-5)

Safety Data

• Hazardous Substances Data: 1265154-01-5(Hazardous Substances Data)

Upstream product

• 766-97-2 4-n-methylphenylacetylene 
• 65-85-0 benzoic acid 
• 536-74-3 phenylacetylene 
• 99511-02-1 (Z)-2-bromo-1-phenylethylene acetate 

Downstream Products

• 119492-83-0 2-(4-Methoxyphenyl)-5-phenylfuran 

Relevant articles and documents

Gold-Catalyzed Regio- and Stereoselective Addition of Carboxylic Acids to Iodoalkynes: Access to (Z)-β-Iodoenol Esters and 1,4-Disubstituted (Z)-Enynyl Esters

In the presence of catalytic amounts of the Au(I) cation [Au(PPh3)]+, a large variety of (Z)-β-iodoenol esters (39 examples) could be synthesized under mild reaction conditions through the regio- and stereospecific intermolecular add

Synthesis of 2,5-disubstituted 3-iodofurans via palladium-catalyzed coupling and iodocyclization of terminal alkynes

2,5-Disubstituted 3-iodofurans are readily prepared under very mild reaction conditions by the palladium/copper-catalyzed cross-coupling of (Z)-β-bromoenol acetates and terminal alkynes, followed by iodocyclization. The useful intermediates conjugated eny