96530-26-6

Basic information

• Product Name: 3-Penten-2-one, 1-(phenylsulfonyl)-, (3E)-
• CAS NO: 96530-26-6
• Molecular Formula: C11H12O3S
• Molecular Weight: 224.28
• Mol File: 96530-26-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-Penten-2-one, 1-(phenylsulfonyl)-, (3E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Penten-2-one, 1-(phenylsulfonyl)-, (3E)-(96530-26-6)
• EPA Substance Registry System: 3-Penten-2-one, 1-(phenylsulfonyl)-, (3E)-(96530-26-6)

Safety Data

• Hazardous Substances Data: 96530-26-6(Hazardous Substances Data)

Upstream product

• 3112-85-4 methylphenylsulfonate 
• 1193-82-4 racemic methyl phenyl sulfoxide 
• 5000-44-2 1-phenylsulfonyl-2-propanone 
• 155259-49-7 1-phenylsulfonyl-4-hydroxy-pentan-2-one 
• 130942-23-3 (3E)-1-Phenylsulfinyl-2-oxo-3-pentene 
• 623-43-8 crotonic acid methyl ester 

Downstream Products

• 96530-31-3 (E)-1-Benzenesulfonyl-6-cyclopropyl-hex-3-en-2-one 
• 96530-36-8 1-Benzenesulfonyl-3-cyclopropylmethyl-pent-4-en-2-one 
• 130942-25-5 8aβ-Carbomethoxy-7-methyl-5-phenylsulfonyl-2,3,4,4a,5,7,8,8a-octahydronaphthalene-1,6-dione 
• 161420-34-4 (2R,4R)-6-Benzenesulfonylmethyl-2-isopropoxy-4-methyl-3,4-dihydro-2H-pyran 
• 96530-29-9 (E)-3-Benzenesulfonyl-non-5-en-4-one 
• 161713-91-3 (5S,6R)-6-methyl-5-(phenylsulfonylacetyl)bicyclo[2.2.1]hept-2-ene 
• 96530-27-7 (E)-5-Benzenesulfonyl-hept-2-en-4-one 
• 96530-28-8 (E)-1-Benzenesulfonyl-hept-3-en-2-one 
• 96530-30-2 (E)-1-Benzenesulfonyl-non-3-en-2-one 
• 96530-35-7 1-Benzenesulfonyl-3-vinyl-heptan-2-one 
• 96530-32-4 (E)-1-Benzenesulfonyl-7-methyl-octa-3,7-dien-2-one 
• 96530-37-9 1-Benzenesulfonyl-5-methyl-3-vinyl-hex-5-en-2-one 
• 96530-33-5 (E)-1-Benzenesulfonyl-6-methyl-hept-3-en-2-one 
• 96530-34-6 1-Benzenesulfonyl-3-isopropyl-pent-4-en-2-one 

Relevant articles and documents

Asymmetric diels-alder reactions of sulfonyl-functionalized α,β-unsaturated ketones with cyclopentadiene catalyzed by chiral lewis acid

Asymmetric Diels-Alder reactions of (E)-1-substituted sulfonyl-3-penten-2- ones with cyclopentadiene catalyzed by a chiral titanium reagent were investigated. The enantioselectivity was studied with different substituents in the position of sulfonyl moiet

(E)-2-Oxo-1-sulfonyl-3-alkenes as Reactive Hetero 1,3-Dienes. Absolutely endo-Selective Hetero Diels-Alder Reactions with Vinyl Ethers in the Presence of a Lewis Acid Catalyst

(E)-2-Oxo-1-sulfonyl-3-alkenes as new hetero 1,3-dienes undergo smooth hetero Diels-Alder reactions with vinyl ethers in the presence of Eu(fod)3 or TiCl2(i-PrO)2.The reactions are absolutely endo-selective producing 2,4-cis-3,4-dihydro-2H-pyrans in excel

Highly stereoselective double Michael cyclization of 1-phenylsulfinyl and sulfonyl analogues of the nazarov reagent

The base-catalyzed double Michael addition of the β-keto sulfoxide 5 with 2-carbomethoxy-2-cyclohexenone (1) proceeds, after elimination of the sulfoxide moiety during chromatography on silica, to give the dehydrodecalin adduct 6 with high stereoselectivi