141037-91-4

Basic information

• Product Name: 1-Propanone, 1-(2-furanyl)-3-hydroxy-3-phenyl-
• CAS NO: 141037-91-4
• Molecular Formula: C13H12O3
• Molecular Weight: 216.236
• Mol File: 141037-91-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(2-furanyl)-3-hydroxy-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(2-furanyl)-3-hydroxy-3-phenyl-(141037-91-4)
• EPA Substance Registry System: 1-Propanone, 1-(2-furanyl)-3-hydroxy-3-phenyl-(141037-91-4)

Safety Data

• Hazardous Substances Data: 141037-91-4(Hazardous Substances Data)

Upstream product

• 141054-35-5 1-(2-furyl)-3-phenyl-3-<(trimethylsilyl)oxy>propan-1-one 
• 62889-08-1 1-(2-furyl)-1-(trimethylsilyloxy)ethylene 
• 100-52-7 benzaldehyde 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 98-01-1 furfural 
• 100-42-5 styrene 
• 3988-74-7 1-(2-furyl)-3-phenylpropen-1-one 

Downstream Products

• 3988-74-7 1-(2-furyl)-3-phenylpropen-1-one 

Relevant articles and documents

Cross aldolization reactions in furane series by means of silyl enol ethers

The catalytic cross aldol reaction between a silyl enol ether and an aldehyde has been applied to the furane series giving the ketols RCOCH2CHOHR' (R or R' = 2-furyl). Good results (with no resinification or crotonisation) have been obtained using bismuth

Vanadyl species-catalyzed complementary β-oxidative carbonylation of styrene derivatives with aldehydes

A series of oxometallic species and metal acetylacetonates (acac) was examined as catalysts for oxidative carbonylation of styrene with benzaldehyde using t-butylhydroperoxide as the co-oxidant in warm acetonitrile. Among them, VO((acac)2 and vanadyl(iv) chloride were found to be the only catalyst class to achieve cross-coupling processes by judiciously tuning the ligand electronic attributes, leading to β-hydroxylation- and β-peroxidation-carbonylation of styrene, respectively, in a complementary manner. Mechanistic studies indicated that vanadyl-associated acyl radicals generated by t-butoxy radical-assisted, homolytic cleavage of the aldehyde C-H bond were involved in tandem processes with an exclusive syn diastereoselectivity in the case of β-methylstyrene. This journal is

Biomimetic hydrogenation: A reusable NADH co-enzyme model for hydrogenation of α,β-epoxy ketones and 1,2-diketones

A biomimetic method has been developed to transform α,β-epoxy ketones or 1,2-diketones into corresponding β-hydroxy ketones or α-hydroxy ketones using a catalytic amount of BNAH or BNA +Br-. The regeneration of BNAH or BNA+Br - is achieved by a mixture of HCOOH/Et3N. A radical mechanism is proposed to explain these observations.