17482-29-0

Basic information

• Product Name: 4-hydroxybutyl p-tolyl sulfone
• Synonyms: 4-hydroxybutyl p-tolyl sulfone
• CAS NO: 17482-29-0
• Molecular Weight: 228.312
• Mol File: 17482-29-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-hydroxybutyl p-tolyl sulfone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxybutyl p-tolyl sulfone(17482-29-0)
• EPA Substance Registry System: 4-hydroxybutyl p-tolyl sulfone(17482-29-0)

Safety Data

• Hazardous Substances Data: 17482-29-0(Hazardous Substances Data)

Upstream product

• 27975-48-0 4-(p-tolylthio)butan-1-ol 
• 127382-67-6 4-<(tert-butyldimethylsilyl)oxy>-1-(p-tolylsulfonyl)butane 
• 133042-97-4 methyl 4-(p-tolylsulfonyl)butanoate 
• 157063-03-1 Acetic acid 4-(toluene-4-sulfonyl)-butyl ester 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 10486-08-5 sodium p-thiocresolate 

Downstream Products

• 127382-69-8 (Z)-4,8-diacetoxy-1-<(tert-butyldimethylsilyl)oxy>-5-(p-tolylsulfonyl)-2-octene 
• 133043-05-7 methyl (1'E,10'S)-2,4-dimethoxy-6-<10'-<(tert-butyldimethylsilyl)oxy>-6'-oxo-5'-(p-tolylsulfonyl)-1'-undecenyl>benzoate 
• 133043-00-2 methyl 2,4-dimethoxy-6-<1'-(p-tolylsulfinyl)-5'-(p-tolylsulfonyl)pentyl>benzoate 
• 133042-99-6 methyl 2,4-dimethoxy-6-<1'-(p-tolylsulfenyl)-5'-(p-tolylsulfonyl)pentyl>benzoate 
• 133043-01-3 methyl (1'E)-2,4-dimethoxy-6-<5'-(p-tolylsulfonyl)-1'-pentenyl>benzoate 
• 157063-04-2 4-(Toluene-4-sulfonyl)-butyraldehyde 

Relevant articles and documents

A versatile approach to cyclic ethers. Synthesis of disubstituted oxepanes and oxocanes

A synthetic sequence for the preparation of α,α'-disubstituted cyclic ethers of various ring sizes and either relative stereochemistry (cis or trans) is presented. It is based on the hetero Diels Alder reaction of a monoactivated diene and an aldehyde, yi

Asymmetric Synthesis of (S)-Zearalenone Dimethyl Ether, an Orsellinic Acid Type Macrolide

The synthesis of (S)-zearalenone dimethyl ether is described.The chiral part of the molecule was obtained by asymmetric synthesis monitored by a chiral sulfoxide group and introduced in the very last steps of the synthesis.

A new method for the stereocontrolled synthesis of silyl dienol ethers using (naphtalene) chromium tricarbonyl catalyzed isomerization

Various tert-butyldimethylsilyl dienol ethers of type 4 were synthesized in a highly stereoselective manner for the first time. Treatment of (1Z)-1-[[(tert-butyldimethylsilyl)oxy] methyl] butadiene derivatives 1 with 20 mol % of (naphthalene) Cr(CO)3