95110-84-2

Basic information

• Product Name: (l)-4-hydroxy-3-methyl-1,4-diphenyl-2-butanone
• CAS NO: 95110-84-2
• Molecular Weight: 254.329
• Mol File: 95110-84-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (l)-4-hydroxy-3-methyl-1,4-diphenyl-2-butanone(CAS DataBase Reference)
• NIST Chemistry Reference: (l)-4-hydroxy-3-methyl-1,4-diphenyl-2-butanone(95110-84-2)
• EPA Substance Registry System: (l)-4-hydroxy-3-methyl-1,4-diphenyl-2-butanone(95110-84-2)

Safety Data

• Hazardous Substances Data: 95110-84-2(Hazardous Substances Data)

Upstream product

• 29626-90-2 1-chloro-2-phenylethyl phenyl sulfoxide 
• 95110-65-9 2,3-epoxy-1-phenyl-2-phenylsulfinylbutane 
• 100-52-7 benzaldehyde 
• 1007-32-5 benzyl ethyl ketone 

Relevant articles and documents

Efficient synthesis of B-iododialkyl- and B-alkyldiiodoboranes as their acetonitrile complexes: Application for the enolboration - Aldolization of ethyl ketones

A series of B-(iododialkyl)boranes and B-(alkyldiiodo)boranes have been readily synthesized as their MeCN complexes from the corresponding chloro- and bromoboranes by treatment with NaI or KI in MeCN. In the presence of EtN(i-Pr)2, the B-(cyclo

Diastereoselective Aldol Addition Using Boron Trichloride or Alkoxydichloroborane

Under carefully controlled conditions, boron trichloride or alkoxytrichloroborane/ethyldiisopropylamine in CH2Cl2 can be used to effect diastereoselective aldol additions of ethyl ketones to saturated, α,β-unsaturated, or aromatic aldehydes.The C-C bond formation takes place with relative topicity ul ('syn' configuration of the aldols), in selectivities ranging from 90 to 99percent ds (Tables 1-3).Mechanistic aspects of the reaction are discussed.