359010-62-1

Basic information

• Product Name: 1,5-di(phenylsulfonyl)-3,7,11-trimethyl-2,6,10-dodecatriene
• Synonyms: 1,5-di(phenylsulfonyl)-3,7,11-trimethyl-2,6,10-dodecatriene
• CAS NO: 359010-62-1
• Molecular Weight: 486.697
• Mol File: 359010-62-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,5-di(phenylsulfonyl)-3,7,11-trimethyl-2,6,10-dodecatriene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-di(phenylsulfonyl)-3,7,11-trimethyl-2,6,10-dodecatriene(359010-62-1)
• EPA Substance Registry System: 1,5-di(phenylsulfonyl)-3,7,11-trimethyl-2,6,10-dodecatriene(359010-62-1)

Safety Data

• Hazardous Substances Data: 359010-62-1(Hazardous Substances Data)

Upstream product

• 359010-60-9 5-phenylsulfonyl-1-phenylthio-3,7,11-trimethyl-2,6,10-dodecatriene 
• 56691-80-6 geranyl phenyl sulfone 
• 57282-70-9 (E)-4-hydroxy-3-methyl-2-butenyl phenyl sulfide 
• 108-98-5 thiophenol 
• 1838-94-4 isoprene epoxide 
• 359010-59-6 4-bromo-3-methyl-2-butenyl phenyl sulfide 

Downstream Products

• 359010-64-3 5,9-di(phenylsulfonyl)-1-phenylthio-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraene 
• 359643-67-7 di(5,9-di(phenylsulfonyl)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl) sulfide 
• 1011506-02-7 (6E,10E)-8,12-bis(benzenesulfonyl)-2,6,10-trimethyldodeca-6,10-dien-2-ol 
• 359643-74-6 Di(5,9-di(phenylsulfonyl)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl) sulfone 
• 359643-76-8 7,7',11,11'-tetra(phenylsulfonyl)-7,7',8,8',11,11',12,12'-octahydrolycopene 
• 359010-65-4 1,5,9-tri(phenylsulfonyl)-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraene 
• 502-65-8 lycopene 

Relevant articles and documents

General preparation and controlled cyclization of acyclic terpenoids

A general preparation method of the all-(E)-polyprenols 12 has been developed from readily available geranyl sulfone by the chain-extension process utilizing the C5 unit 5 and the chain-termination process utilizing the C5 unit 10 to

A highly efficient chain-extension process in the systematic syntheses of carotenoid natural products

Successive elongation by a C5 unit is possible when an allylic sulfone is couple with 4-bromo-3-methyl-2-butenyl phenyl sulfide (1). The thiosulfone compound formed was then oxidized to the corresponding disulfone, which, upon coupling with another equivalent of 1 and oxidation, produced the trisulfone 2, again elongated by a C5 unit (see scheme). This process, which can be repeated again, is the basis for a highly efficiently synthesis of carotenoids.