82912-81-0

Basic information

• Product Name: 1-Butanone, 3-hydroxy-1,3-bis(3-methoxyphenyl)-
• CAS NO: 82912-81-0
• Molecular Formula: C18H20O4
• Molecular Weight: 300.354
• Mol File: 82912-81-0.mol

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 3-hydroxy-1,3-bis(3-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 3-hydroxy-1,3-bis(3-methoxyphenyl)-(82912-81-0)
• EPA Substance Registry System: 1-Butanone, 3-hydroxy-1,3-bis(3-methoxyphenyl)-(82912-81-0)

Safety Data

• Hazardous Substances Data: 82912-81-0(Hazardous Substances Data)

Upstream product

• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 135388-39-5 ((1-(3-methoxyphenyl)vinyl)oxy)trimethylsilane 

Relevant articles and documents

The indium(III) chloride-catalysed hydrolysis and in situ Mukaiyama-type reaction of arylmethyl ketone derived silyl enol ethers under solvent-free conditions

Treatment of trimethylsilyl enol ethers of arylmethyl ketones with catalytic amounts of indium(III) chloride under solvent-free conditions leads to a remarkably efficient process of in situ hydrolysis and Mukaiyama-type addition to the resulting ketones.

Some Aspects of the Reaction of Phenylselenomagnesium Bromide with Carbonyl Compounds

The reactivity of phenylselenomagnesium bromide with some carbonyl compounds has been studied.It was found that aromatic aldehydes were reduced to give the corresponding alcohols, and aliphatic aldehydes and ketones which have active hydrogens were found to afford condensed products.Keywords---reactivity of phenylselenomagnesium bromide; reduction of aromatic aldehydes; condensing agents; organoselenium compounds; synthesis of aromatic alcohols