1434751-60-6

Basic information

• Product Name: 2-benzoyl-4-(4-nitrophenyl)-1-phenylbut-2-ene-1,4-dione
• Synonyms: 2-benzoyl-4-(4-nitrophenyl)-1-phenylbut-2-ene-1,4-dione
• CAS NO: 1434751-60-6
• Molecular Weight: 385.376
• Mol File: 1434751-60-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-benzoyl-4-(4-nitrophenyl)-1-phenylbut-2-ene-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzoyl-4-(4-nitrophenyl)-1-phenylbut-2-ene-1,4-dione(1434751-60-6)
• EPA Substance Registry System: 2-benzoyl-4-(4-nitrophenyl)-1-phenylbut-2-ene-1,4-dione(1434751-60-6)

Safety Data

• Hazardous Substances Data: 1434751-60-6(Hazardous Substances Data)

Upstream product

• 110944-98-4 2-iodo-1-(4-nitrophenyl)ethanone 
• 120-46-7 1,3-diphenylpropanedione 
• 99-81-0 4-Nitrophenacyl bromide 
• 34006-49-0 2-chloro-1-(4-nitrophenyl)ethanone 
• 100-19-6 (4-nitrophenyl)ethanone 

Downstream Products

• 1434752-21-2 2-benzoyl-4-(4-nitrophenyl)-1-phenyl-3-(1H-pyrazol-1-yl)but-2-ene-1,4-dione 
• 5541-64-0 2-(4-nitro-phenyl)-quinoxaline 

Relevant articles and documents

Target-oriented synthesis: Miscellaneous synthetic routes to access 1,4-enediones through the coupling of 1,3-dicarbonyl compounds with multiform substrates

Target-oriented synthetic protocol was presented for the synthesis of 1,4-enediones. The approach can efficiently construct 1,4-enediones through different reaction pathways from multiform substrates α-halo aromatic ketones, 2-hydroxy-aromatic ketones and methyl carbinols. In this reaction, CuI was found to be the most efficient catalyst. Multiform substrates were also found to perform well to afford the products in a one-pot fashion.