88841-83-2

Basic information

• Product Name: 2-Cyclohexen-1-one, 3-(phenylseleno)-
• Synonyms: 3-(phenylseleno)-2-cyclohexenone;3-(Phenylseleno)-2-cyclohexen-1-one;2-Cyclohexen-1-one,3-(phenylseleno);1-phenylselanyl-1-cyclohexen-3-one
• CAS NO: 88841-83-2
• Molecular Formula: C12H12OSe
• Molecular Weight: 251.187
• Mol File: 88841-83-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 3-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 3-(phenylseleno)-(88841-83-2)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 3-(phenylseleno)-(88841-83-2)

Safety Data

• Hazardous Substances Data: 88841-83-2(Hazardous Substances Data)

Upstream product

• 5682-75-7 3-chloro-2-cyclohexenone 
• 23974-72-3 sodium phenylselenide 
• 71712-68-0 Phosphoric acid diethyl ester 3-oxo-cyclohex-1-enyl ester 
• 52251-58-8 lithium phenylselenide 
• 65825-82-3 3-(Phenylsulfonyl)cyclohex-2-en-1-ol 
• 56671-82-0 3-Iodocyclohex-2-enone 
• 1666-13-3 diphenyl diselenide 
• 5707-04-0 Phenylselenyl chloride 
• 163332-59-0 (3-Methoxy-cyclohex-1-enesulfonyl)-benzene 
• 57918-73-7 3-acetoxy-cyclohex-2-enone 
• 33861-17-5 phenyl trimethylsilyl selenide 

Downstream Products

• 6301-49-1 3-butylcyclohexenone 
• 29179-20-2 3-(β-Styryl)-2-cyclohexenone 
• 88841-93-4 1-(3-Hydroxypropyl)-3-(phenylselenonyl)-2-cyclohexen-1-ol 
• 79681-30-4 1-Butyl-3-(phenylselenonyl)-2-cyclohexen-1-ol 
• 56881-77-7 3-(2-methyl-1-propenyl)-2-cyclohexen-1-one 
• 138616-38-3 3-(phenylethynyl)-2-cyclohexen-1-one 
• 60439-28-3 3-Pentyl-2-cyclohexen-1-one 
• 1132-39-4 diphenylselenide 
• 10345-87-6 3-phenylcyclohex-2-enone 
• 37172-14-8 3-(1-methylpropyl)-2-cyclohexen-1-one 
• 17299-35-3 3-(tert-butyl)cyclohex-2-en-1-one 
• 1193-18-6 3-methylcyclohexen-2-one 
• 66262-12-2 3-hexyl-2-cyclohexen-1-one 
• 192815-46-6 ethyl 2-(3-phenylselanyl-2-cyclohexenyliden)acetate 

Relevant articles and documents

Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates

Enol phosphates and enol tosilates of β-dicarbonyl compounds react with lithium organoselenolates to give β-organoseleno (Z)-α,β-unsaturated carbonyl compounds. Tetrasubstituted vinylic vic-bis(organylchalcogenides) of (E)-geometry have been prepared by t

A highly efficient synthesis of β-substituted six- and seven-membered-ring enones via carbon alkylation of γ-methoxy allylsulfonyl anions

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Reactions of 3-Hydroxyvinyl Selenones with Alkoxides. Oxetane Formation and Fragmentation Reactions

3-Hydroxyvinyl phenyl selenones are prepared and their behavior as conjugate addition acceptors has been investigated.As a result, a selenonyl group has been found to activate the C=C bond for conjugate addition of nucleophiles and further to behave as an