108415-83-4

Basic information

• Product Name: (E)-β-styryl phenyl selenone
• Synonyms: (E)-β-styryl phenyl selenone
• CAS NO: 108415-83-4
• Molecular Weight: 291.208
• Mol File: 108415-83-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-β-styryl phenyl selenone(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-β-styryl phenyl selenone(108415-83-4)
• EPA Substance Registry System: (E)-β-styryl phenyl selenone(108415-83-4)

Safety Data

• Hazardous Substances Data: 108415-83-4(Hazardous Substances Data)

Upstream product

• 60466-40-2 (E)-phenyl(styryl)selane 

Downstream Products

• 96-09-3 styrene oxide 
• 4747-13-1 α-methoxystyrene 
• 4110-75-2 (E)-(2-methoxyvinyl)benzene 
• 72204-02-5 (1R,2R)-1,2-diphenylcyclopropanecarbonitrile 
• 87421-66-7 (1S,2S)-(-)-1,2-diphenylcyclopropanecarbonitrile 
• 1180679-02-0 ethyl 2-cyano-2,3-diphenyl-4-(phenylselenonyl)-butanoate 
• 1203602-52-1 isopropyl 2-cyano-2,3-diphenyl-4-(phenylselenonyl)-butanoate 
• 1203602-51-0 benzyl 2-cyano-2,3-diphenyl-4-(phenylselenonyl)-butanoate 
• 27159-38-2 N-benzyl-2-phenylaziridine 
• 27159-38-2 (R)-(-)-N-Benzyl-2-phenylaziridine 
• 1244770-97-5 methyl (2-phenyl-1-aziridinyl)acetate 
• 815576-08-0 (+/-)-1-allyl-2-phenylaziridine 
• 1244770-94-2 4-(2-phenyl-1-aziridinyl)butylamine 
• 136912-53-3 1-butyl-2-phenylaziridine 

Relevant articles and documents

Oxone-Mediated Oxidation of Vinyl Selenides in Water

A simple and practical procedure for the oxidation of vinyl selenides into the corresponding selenones using Oxone in water at 60 °C has been reported. Structurally diverse phenyl vinyl selenones were oxidized under heterogeneous conditions without organi

COMPETITION BETWEEN VINYLIC SUBSTITUTION AND CONJUGATE ADDITION IN THE REACTIONS OF VINYL SELENOXIDES AND VINYL SELENONES WITH NUCLEOPHILES IN DMF

Vinyl selenoxides and vinyl selenones present a different reactivity towards thiolate or alkoxide anions in DMF.In the case of selenoxides the addition of the nucleophiles regioselectively occurs at the α-carbon leading to the formation of the vinylic sub