1100356-99-7

Basic information

• Product Name: (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyl-9,17-bis[(4-methylphenyl)sulfonyl]dotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl acetate
• Synonyms: (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyl-9,17-bis[(4-methylphenyl)sulfonyl]dotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl acetate
• CAS NO: 1100356-99-7
• Molecular Weight: 913.38
• Mol File: 1100356-99-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyl-9,17-bis[(4-methylphenyl)sulfonyl]dotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyl-9,17-bis[(4-methylphenyl)sulfonyl]dotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl acetate(1100356-99-7)
• EPA Substance Registry System: (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyl-9,17-bis[(4-methylphenyl)sulfonyl]dotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl acetate(1100356-99-7)

Safety Data

• Hazardous Substances Data: 1100356-99-7(Hazardous Substances Data)

Upstream product

• 51921-98-3 (4E,8E)-ethyl 2-acetyl-5,9,13-trimethyltetradeca-4,8,12-trienoate 
• 50848-64-1 2E,6E,10E-geranylgeranyl bromide 
• 24034-73-9 Geranylgeraniol 
• 24035-35-6 (2E,6E,10E)-3,7,11,15-tetramethyl-hexadeca-2,6,10,14-tetraenoic acid ethyl ester 
• 1117-52-8 6,10,14-trimethyl-5,9,13-pentadecatriene-2-on 
• 24163-93-7 farnesyl bromide 
• 106-28-5 Farnesol 
• 1100356-96-4 (2E,6E,10E,14E)-16-bromo-3,7,11,15-tetramethyl-9-[(4-methylphenyl)sulfonyl]hexadeca-2,6,10,14-tetraen-1-yl acetate 
• 68690-47-1 1-methyl-4-{[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]sulfonyl}benzene 

Downstream Products

• 1100357-00-3 C₅₄H₇₈O₅S₂ 
• 33569-79-8 (2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-ol 

Relevant articles and documents

A convergent stereocontrolled synthesis of [3-14C]solanesol

In this communication, we report the synthesis of 5 mCi of [3- 14C]solanesol (1) prepared from ethyl [3-14C]acetoacetate and (all-E)-octaprenyl bromide (2) in four steps, with a specific radioactivity of 19.83 mCi/mmol and with a chemical/ stereochemical and radiochemical purity of ≥ 95%. (Figure 1). Position 3 of the chain was selected for 14C labelling because of the metabolic stability of this position. Unlabelled (all-E)-octaprenyl (18) (Scheme 4) necessary for this work was prepared via a convergent iterative 'allyl-allyl' coupling approach of precursors easily derived from readily available inexpensive starting materials. Copyright