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

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

• 65-85-0 benzoic acid 
• 766-97-2 4-n-methylphenylacetylene 
• 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

A highly efficient synthesis of 2,5-disubstituted furans from enyne acetates catalyzed by lewis acid and palladium

A highly efficient synthesis of a wide range of 2,5-disubstituted furans from enyne acetates is described. The reactions are conducted by using Lewis acid and palladium catalyst and provide symmetrical and unsymmetrical products in good to excellent yields, with broad substrate scope, including a variety of aromatic and aliphatic substituents in the 2- and 5-position of the furan ring.

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