1244029-98-8

Basic information

• Product Name: (E)-2-(2-n-butyl-2-(2-n-butylbenzofuran-3-yl)vinyl)phenol
• Synonyms: (E)-2-(2-n-butyl-2-(2-n-butylbenzofuran-3-yl)vinyl)phenol
• CAS NO: 1244029-98-8
• Molecular Weight: 348.485
• Mol File: 1244029-98-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-2-(2-n-butyl-2-(2-n-butylbenzofuran-3-yl)vinyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(2-n-butyl-2-(2-n-butylbenzofuran-3-yl)vinyl)phenol(1244029-98-8)
• EPA Substance Registry System: (E)-2-(2-n-butyl-2-(2-n-butylbenzofuran-3-yl)vinyl)phenol(1244029-98-8)

Safety Data

• Hazardous Substances Data: 1244029-98-8(Hazardous Substances Data)

Upstream product

• 125345-27-9 2-(hex-1-yn-1-yl)phenol 
• 930-68-7 cyclohexenone 

Relevant articles and documents

Domino rhodium(I)-catalysed reactions for the efficient synthesis of substituted benzofurans and indoles

Rhodium(I) catalysts promote the transformation of o-alkynyl phenols and anilines to the corresponding benzo[b]furans and indoles. The reaction is postulated to proceed via a transient 3-rhodium heterocycle intermediate, which can be trapped with suitable electrophiles to give poly-substituted heterocycles. In the case of mono-substituted electron-withdrawn electrophiles, excellent yield and selectivity for conjugate addition versus Heck-Mizoroki reaction can be achieved. In the case of 2-alkynyl pyridine electrophiles, novel 2-(benzofuran-3-yl)vinylpyridines are formed.