38818-91-6

Basic information

• Product Name: (((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)sulfonyl)benzene
• Synonyms: (((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)sulfonyl)benzene
• CAS NO: 38818-91-6
• Molecular Weight: 414.653
• Mol File: 38818-91-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)sulfonyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)sulfonyl)benzene(38818-91-6)
• EPA Substance Registry System: (((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)sulfonyl)benzene(38818-91-6)

Safety Data

• Hazardous Substances Data: 38818-91-6(Hazardous Substances Data)

Upstream product

• 57804-27-0 [(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl](phenyl)sulfane 
• 24034-73-9 Geranylgeraniol 
• 873-55-2 sodium benzenesulfonate 
• 42207-88-5 (2E,6E,10E)-methyl 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoate 
• 1117-52-8 6,10,14-trimethyl-5,9,13-pentadecatriene-2-on 
• 108-98-5 thiophenol 
• 50848-64-1 2E,6E,10E-geranylgeranyl bromide 

Downstream Products

• 1011506-00-5 (2E,6E,10E)-5-(benzenesulfonyl)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl phenyl sulfide 
• 116059-40-6 Acetic acid (3E,7E,11E)-2-benzenesulfonyl-4,8,12,16-tetramethyl-1-((1E,5E,9E)-2,6,10,14-tetramethyl-pentadeca-1,5,9,13-tetraenyl)-heptadeca-3,7,11,15-tetraenyl ester 
• 116059-44-0 ((6E,10E,14E,16Z,18E,22E,26E)-2,6,10,14,19,23,27,31-Octamethyl-dotriaconta-2,6,10,14,16,18,22,26,30-nonaene-16-sulfonyl)-benzene 
• 540-04-5 phytoene 
• 116059-54-2 (6E,10E,14E,18E,22E,26E)-17-Benzenesulfonyl-2,6,10,14,19,23,27,31-octamethyl-dotriaconta-2,6,10,14,18,22,26,30-octaen-16-ol 

Relevant articles and documents

Development of a new air-stable structure-simplified nafuredin-γ analog as a potent and selective nematode complex I inhibitor

Nafuredin-γ, obtained from natural nafuredin, has demonstrated a potent and selective inhibitory activity against nematode complex I. However, nafuredin-γ is unstable in air since its conjugated dienes are oxygen-labile. The instability in air was natural

Superacidic low temperature cyclization of terpenylphenyisulfones

The superacidic cyclization of aliphatic and partially cyclized C10- C20 terpenylphenylsulfones proceeds structure-selectively and stereospecifically, affording α- or mixtures of α- and γ-isomers of completely cyclized terpenylphenylsulfones. The configuration of the phenylsuffonylmethylene group in the cyclized products is predetermined by the configuration of the allylic double bond in the starting compounds.