72863-23-1

Basic information

• Product Name: 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene
• Synonyms: 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene
• CAS NO: 72863-23-1
• Molecular Weight: 292.442
• Mol File: 72863-23-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene(72863-23-1)
• EPA Substance Registry System: 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene(72863-23-1)

Safety Data

• Hazardous Substances Data: 72863-23-1(Hazardous Substances Data)

Upstream product

• 115-95-7 linalool acetate 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 106-24-1 Geraniol 
• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 119306-02-4 geranyl p-toluenesulfinate 
• 119784-71-3 5-<(E)-3,7-dimethyl-2,6-octadienylthio>-1-phenyl-1H-tetrazole 
• 105-87-3 3,7-dimethyl-2E,6-octadien-1-yl acetate 
• 141-12-8 neryl acetate 
• 123-35-3 7-methyl-3-methene-1,6-octadiene 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 68690-44-8 neryl p-tolyl sulfone 
• 53254-60-7 3,7-dimethyl-1-(p-toluenesulfonyl)-2(E),6-octadiene 
• 83110-46-7 3,7-dimethyl-1-(p-tolylsulfonyl)-2,6-octadiene 
• 110109-67-6 3,7-dimethyl-3-p-toluenesulfonyl-1-octene 
• 110109-66-5 7-chloro-3,7-dimethyl-3-(p-toluene sulfonyl)-1-octene 
• 19894-79-2 diethyl [(2E)-3,7-dimethylocta-2,6-dienyl]malonate 
• 37606-77-2 (2Z)-diethyl (3,7-dimethyl-2,6-octadienyl)malonate 
• 99372-02-8 2-(1,5-Dimethyl-1-vinyl-hex-4-enyl)-malonic acid diethyl ester 
• 51361-62-7 (E)-3-Benzenesulfonyl-6,10-dimethyl-undeca-5,9-dien-2-one 
• 31162-76-2 (cis-3,7-Dimethyl-2,6-octadienyl) phenyl sulfide 
• 35162-74-4 geranyl phenyl sulfide 
• 21488-83-5 (2E)-1-phenyl-3,7-dimethyl-2,6-octadiene 
• 21488-83-5 (2Z)-1-Phenyl-3,7-dimethyl-2,6-octadiene 

Relevant articles and documents

Convenient synthesis of allylic sulfides and application to allylic carbon-carbon bond formation

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Asymmetric Induction Reactions. III. Palladium-Catalyzed Asymmetric Sulfonylations of Allylic Sulfinates and Acetates with Chiral Phosphine Ligands

Treatment of allylic (+/-)-p-toluenesulfinate with tetrakis(triphenlphosphine)palladium in the presence of chiral phosphine ligands resulted in allylic sulfinate-sulfone rearrangements to give the corresponding optically active allylic sulfones in high op

SYNTHESES A L'AIDE DE SULFONES. XXIII. SUR LA SELECTIVITE DE LA SYNTHESE DES DULFONES ALLYLIQUES

The role of the palladium ligands on the yield and regioselectivity of the reaction of conjugated dienes with arenesulphinic acids (or of allylic acetates with sodium arenesulphinates) has been investigated.Arenesulphinic acids catalyse the isomerisation of allylic sulphones.