74829-78-0

Basic information

• Product Name: Benzene, 1-methyl-4-(1-pentenylsulfonyl)-, (E)-
• CAS NO: 74829-78-0
• Molecular Formula: C12H16O2S
• Molecular Weight: 224.324
• Mol File: 74829-78-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methyl-4-(1-pentenylsulfonyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methyl-4-(1-pentenylsulfonyl)-, (E)-(74829-78-0)
• EPA Substance Registry System: Benzene, 1-methyl-4-(1-pentenylsulfonyl)-, (E)-(74829-78-0)

Safety Data

• Hazardous Substances Data: 74829-78-0(Hazardous Substances Data)

Upstream product

• 3185-99-7 Methyl p-tolyl sulfone 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 7257-26-3 sodium p-toluenesulfinate tetrahydrate 
• 109-65-9 1-bromo-butane 
• 7569-26-8 chloromethyl p-tolylsulfone 
• 37891-95-5 bromomethyl 4-tolyl sulfone 
• 139950-90-6 2-(1-pyrrolidinyl)-1-tosylpentane 
• 36525-00-5 chloro-pent-1-en-t-yl-mercury 
• 109-67-1 1-penten 

Downstream Products

• 1239456-65-5 (E)-N-(2-methyl-3-phenyl-1-propylprop-2-enyl)-4-methylphenylsulfonamide 
• 105235-58-3 (Z)-1-tosyl-2-pentene 
• 72863-25-3 (E)-1-tosyl-2-pentene 
• 72863-25-3 1-Methyl-4-[((E)-pent-2-ene)-1-sulfonyl]-benzene 

Relevant articles and documents

Ir-Catalyzed Remote Functionalization by the Combination of Deconjugative Chain-Walking and C-H Activation Using a Transient Directing Group

An Ir-catalyzed reaction of N-benzylideneanilines with functionalized alkenes such as α,β-unsaturated esters gave ortho-substituted benzaldehyde derivatives with a functional group at the remote position after acidic treatment. The present transformation

Facile method for solid-phase synthesis of vinyl sulfones using polystyrene-supported selenomethyl aryl sulfone

Treatment of novel polystyrene-supported selenomethyl aryl sulfone with LDA followed by alkylation and oxidation elimination efficiently afforded vinyl sulfones in good yields and purities.

Abnormal Four-Membered Ring Formation in Intramolecular Radicalic Cyclization. High Stability of the Alkyl Radical Substituted with Methylthio and p-Tolylsulfonyl Groups

Treatment of 5-iodo-1-(methylthio)-1-(p-tolylsulfonyl)-1-pentene with (n-Bu)3SnH and AIBN gave cyclobutane.This is due to the stability of an intermediary radical attached to methylthio and p-tolylsulfonyl groups.