30506-39-9

Basic information

• Product Name: phenyl 1-octyl sulfoxide
• Synonyms: phenyl 1-octyl sulfoxide
• CAS NO: 30506-39-9
• Molecular Weight: 238.394
• Mol File: 30506-39-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: phenyl 1-octyl sulfoxide(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 1-octyl sulfoxide(30506-39-9)
• EPA Substance Registry System: phenyl 1-octyl sulfoxide(30506-39-9)

Safety Data

• Hazardous Substances Data: 30506-39-9(Hazardous Substances Data)

Upstream product

• 111-66-0 oct-1-ene 
• 108-98-5 thiophenol 
• 1070-00-4 trioctylaluminum 
• 98-09-9 benzenesulfonyl chloride 
• 13910-16-2 n-octylsulfanylbenzene 
• 75-05-8 acetonitrile 

Downstream Products

• 75717-41-8 (Z)-oct-1-enylsulfanyl-benzene 
• 75717-40-7 (E)-oct-1-enylsulfanyl-benzene 
• 98750-72-2 (1,2-Dichloro-octylsulfanyl)-benzene 
• 13910-16-2 n-octylsulfanylbenzene 

Relevant articles and documents

Acid-Catalyzed Oxidative Addition of Thiols to Olefins and Alkynes for a One-Pot Entry to Sulfoxides

An oxidative variant of the thiol-ene reaction has been developed, achieving the direct addition of thiols to olefins to form sulfoxides. The reaction uses tert-butyl hydroperoxide as oxidant and methanesulfonic acid as catalyst. The latter is believed to catalyze the oxidation of the intermediate sulfide to the sulfoxide. No special precautions are necessary to exclude oxygen, yet the products are formed without oxidation at the β-position. Styrenes, acrylic acid derivatives, alkynes, and thiophenols gave the highest yields, while aliphatic olefins and thiols were less effective.

Metal-Free Bacterial Haloperoxidases as Unusual Hydrolases: Activation of H2O2 by the Formation of Peracetic Acid

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Oxidation of thioethers by manganese(IV) oxide-trimethylchlorosilane

Thioethers are transformed by manganese(IV) oxide-trimethylchlorosilane in CH3OH in high yields to sulphoxides, exclusively.