67515-50-8

Basic information

• Product Name: 3,4-Pentadien-2-one, 3-methyl-1-phenyl-
• CAS NO: 67515-50-8
• Molecular Formula: C12H12O
• Molecular Weight: 172.227
• Mol File: 67515-50-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4-Pentadien-2-one, 3-methyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Pentadien-2-one, 3-methyl-1-phenyl-(67515-50-8)
• EPA Substance Registry System: 3,4-Pentadien-2-one, 3-methyl-1-phenyl-(67515-50-8)

Safety Data

• Hazardous Substances Data: 67515-50-8(Hazardous Substances Data)

Upstream product

• 122-78-1 phenylacetaldehyde 
• 3355-28-0 1-Bromo-2-butyne 

Downstream Products

• 1571070-64-8 3,4-dimethyl-1-phenyl-1H-quinolizin-2(9aH)-one 
• 1571071-00-5 3,4-dimethyl-1-phenyl-2H-quinolizin-2-one 
• 1571070-79-5 3,4,6-trimethyl-1-phenyl-1H-quinolizin-2(9aH)-one 
• 1571071-05-0 3,4,8-trimethyl-1-phenyl-2H-quinolizin-2-one 
• 1571070-87-5 3,4-dimethyl-1-phenyl-1H-pyrido[2,1-a]isoquinolin-2(11bH)-one 
• 1571071-08-3 8-methoxy-3,4-dimethyl-1-phenyl-2H-quinolizin-2-one 
• 1590402-97-3 (4-fluorophenyl)(1,2,7-trimethylindolizin-3-yl)methanone 
• 1590402-95-1 (3-chlorophenyl)(1,2,7-trimethylindolizin-3-yl)methanone 
• 1590402-93-9 (4-methoxyphenyl)(1,2,7-trimethylindolizin-3-yl)methanone 

Relevant articles and documents

Sustainable and selective synthesis of 3,4-dihydroquinolizin-2-one and quinolizin-2-one derivatives via the reactions of penta-3,4-dien-2-ones

In this paper, a novel and green methodology for the synthesis of 3,4-dihydroquinolizin-2-one derivatives via the tandem reactions of penta-3,4-dien-2-ones with pyridine, quinoline, or isoquinoline at rt in aqueous ethanol was developed. Notably, the reac

Studies on the Himbert intramolecular arene/allene diels-alder cycloaddition. Mechanistic studies and expansion of scope to all-carbon tethers

The unusual intramolecular arene/allene cycloaddition described 30 years ago by Himbert permits rapid access to strained polycyclic compounds that offer great potential for the synthesis of complex scaffolds. To more fully understand the mechanism of this