53931-59-2

Basic information

• Product Name: 1-Penten-3-one, 5-phenyl-
• CAS NO: 53931-59-2
• Molecular Formula: C11H12O
• Molecular Weight: 160.216
• Mol File: 53931-59-2.mol
• Article Data: 38

Chemical Properties

• CAS DataBase Reference: 1-Penten-3-one, 5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Penten-3-one, 5-phenyl-(53931-59-2)
• EPA Substance Registry System: 1-Penten-3-one, 5-phenyl-(53931-59-2)

Safety Data

• Hazardous Substances Data: 53931-59-2(Hazardous Substances Data)

Upstream product

• 16900-77-9 5-phenyl-2-pentynol 
• 50-00-0 formaldehyd 
• 16520-62-0 4-Phenyl-1-butyne 
• 1275874-85-5 N-methoxy-3-(p-tolyl)-N-methylpropanamide 
• 1826-67-1 vinyl magnesium bromide 
• 37904-38-4 5-phenylpent-1-en-3-ol 
• 122-97-4 3-Phenyl-1-propanol 
• 170646-96-5 N-methoxy-N-methyl-3-phenylpropionamide 
• 104-53-0 3-phenyl-propionaldehyde 
• 100-39-0 benzyl bromide 
• 79141-02-9 3-Phenethyl-5,6-dihydro-4H-[1,2]oxazine 
• 136068-05-8 1-(2-phenylethyl)cyclopropanol 
• 17077-46-2 4-(3-phenyl-propionyl)-morpholine 
• 76837-23-5 2-(2-Phenylethyl)-2-triethylsiloxy-3-butennitril 

Downstream Products

• 121175-02-8 2-Methoxy-5,7,8-trimethyl-2-phenethyl-chroman-6-ol 
• 70280-39-6 1-Hydroxy-2-methyl-1,5-diphenyl-pentan-3-one 
• 1110631-02-1 C₁₆H₂₂O 
• 1253956-41-0 (4E,7R)-8-(1,3-dithian-2-yl)-1-phenyl-7-[(triethylsilyl)oxy]oct-4-en-3-one 
• 1253956-37-4 (4E,7R)-7-{[tert-butyl(dimethyl)silyl]oxy}-9-[(4-methoxybenzyl)oxy]-1-phenylnon-4-en-3-one 
• 1255940-70-5 [InCl(C₆H₅CH₂CH₂COCH₂CH₂)2] 
• 1309477-00-6 (E)-6-(2-(t-butyldimethylsilyloxy)phenyl)-1-phenylhex-4-en-3-one 

Relevant articles and documents

Silver oxide(I) promoted Conia-ene/radical cyclization for a straightforward access to furan derivatives

A novel access to fused furan cores using silver oxide(I) has been developed. Mechanistic investigations indicate the involvement of a Conia-ene reaction/radical cyclization for an expedient path to complex furan derivatives. The reaction is broad in scop

Nickel-Catalyzed C(sp3)-H Functionalization of Benzyl Nitriles: Direct Michael Addition to Terminal Vinyl Ketones

An efficient nickel(0)-catalyzed addition of benzyl nitriles to terminal vinyl ketones via C(sp3)-H functionalization has been developed. The reaction provides a novel and efficient protocol for the synthesis of α-functionalized benzyl nitriles with a wide range of structural diversity under mild reaction conditions while obviating the use of a strong base. The work might be potentially useful toward the development of an enantioselective variant using chiral nitrogen ligands.

Generation of α-Boryl Radicals and Their Conjugate Addition to Enones: Transition-Metal-Free Alkylation of gem-Diborylalkanes

A transition-metal-free method for the alkylation of gem-diborylalkanes with α,β-unsaturated ketones has been developed. It is demonstrated that the α-boryl radicals can be generated efficiently from gem-diborylalkanes with the aid of catechol and oxidants. The α-boryl radicals formed through such process can be engaged in conjugate addition reaction with α,β-unsaturated ketones. This transformation is a straightforward method for the synthesis of γ-borylketones.