123507-32-4

Basic information

• Product Name: 2-hydroxy-1-phenyl-pent-4-en-1-one
• Synonyms: 2-hydroxy-1-phenyl-pent-4-en-1-one
• CAS NO: 123507-32-4
• Molecular Weight: 176.215
• Mol File: 123507-32-4.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 2-hydroxy-1-phenyl-pent-4-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxy-1-phenyl-pent-4-en-1-one(123507-32-4)
• EPA Substance Registry System: 2-hydroxy-1-phenyl-pent-4-en-1-one(123507-32-4)

Safety Data

• Hazardous Substances Data: 123507-32-4(Hazardous Substances Data)

Upstream product

• 1074-12-0 phenylglyoxal hydrate 
• 762-72-1 allyl-trimethyl-silane 
• 1075-06-5 2,2-dihydroxy-1-phenyl-ethanone 
• 24850-33-7 allyltributylstanane 
• 7393-43-3 tetraallyl tin 
• 106-95-6 allyl bromide 
• 28922-53-4 allylmercury bromide 
• 2097-71-4 diallylmercury 
• 1793-91-5 tetraallylgermanium 
• 1730-25-2 allylmagnesium bromide 
• 78146-52-8 phenylglyoxal monohydrate 
• 107-18-6 allyl alcohol 
• 123507-31-3 1-(Dimethyl-hydrazono)-1-phenyl-pent-4-en-2-ol 
• 762-73-2 trimethyl(allyl)stannane 

Downstream Products

• 1051946-18-9 C₂₀H₂₀O₄ 

Relevant articles and documents

Scandium trifluoromethanesulfonate-catalyzed chemoselective allylation reactions carbonyl compounds with tetraallylgermane in aqueous media

Scandium(III) triflate-catalyzed allylation of carbonyl compounds with tetraallylgermane proceeded readily in aqueous nitromethane to afford homoallyl alcohols in excellent to good yields. The presence of H2O is indispensable far the allylation of aldehydes to proceed smoothly. Aldehydes were allylated exclusively in the presence of ketone moieties.

Organic synthesis in solid media. Silica gel as an effective and reusable medium for the selective allylation of aldehydes with tetraallyltin

Wet silica gel promotes the chemoselective and almost complete allylation of aldehydes with 0.25-0.30 molar equivalents of tetraallyltin without an organic solvent, leaving no organotin compounds, requiring neither extraction nor chromatographic separatio

Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes

Cationic cobalt porphyrin-catalyzed allylation of aldehydes with allyltrimethylsilanes is developed. The formation of the aldehyde-cobalt porphyrin complex, the key intermediate for the addition of allylsilanes, is confirmed by theoretical studies and syn

Ceric(IV) ammonium nitrate: A novel reagent for the synthesis of homoallyl alcohols

A rapid and highly efficient method has been developed for the allylation of aldehydes with allyltributylstannane using a catalytic amount of eerie ammonium nitrate in acetonitrile under mild and neutral conditions to afford the corresponding homoallyl al