59057-12-4

Basic information

• Product Name: 5-(2'.6'.6'.-trimethyl-1'-cyclohexenyl)-1-benzenesulphonyl-3-methyl 2.4-pentadiene
• Synonyms: 5-(2'.6'.6'.-trimethyl-1'-cyclohexenyl)-1-benzenesulphonyl-3-methyl 2.4-pentadiene
• CAS NO: 59057-12-4
• Molecular Weight: 344.518
• Mol File: 59057-12-4.mol

Chemical Properties

• CAS DataBase Reference: 5-(2'.6'.6'.-trimethyl-1'-cyclohexenyl)-1-benzenesulphonyl-3-methyl 2.4-pentadiene(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2'.6'.6'.-trimethyl-1'-cyclohexenyl)-1-benzenesulphonyl-3-methyl 2.4-pentadiene(59057-12-4)
• EPA Substance Registry System: 5-(2'.6'.6'.-trimethyl-1'-cyclohexenyl)-1-benzenesulphonyl-3-methyl 2.4-pentadiene(59057-12-4)

Safety Data

• Hazardous Substances Data: 59057-12-4(Hazardous Substances Data)

Upstream product

• 134436-09-2 [(2E,4E)-1-Benzenesulfonyl-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienyl]-trimethyl-silane 
• 79-77-6 (E)-β-ionone 
• 56691-74-8 {[(2,6,6-trimethyl-1-cyclohexen-1-yl)methyl]sulfonyl}benzene 
• 59057-30-6 (1E)-1-(2,6,6-trimethylcyclohex-1-enyl)-3-methyl-1,4-pentadien-3-ol 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 134436-06-9 [(2E,4E)-3-methyl-5-(2,6,6-trimethyl-1-cyclohexenyl)-2,4-pentadienyl]trimethylsilane 
• 134436-07-0 Trimethyl-[(2Z,4E)-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienyl]-silane 
• 51468-89-4 1,3,3-trimethyl-2-[(1E,3E)-3-methyl-1,3-pentadienyl]cyclohexene 

Relevant articles and documents

Allylic sulfones containing triene moieties as key synthons for carotenoid synthesis

An efficient synthetic method for the allylic sulfone 2 containing a conjugated triene moiety has been proposed involving i) coupling of allylic sulfones 4 with the C5 bromoallylic sulfide 5, ii) base-promoted dehydrosulfonation in the presence of allylic sulfide, and iii) selective oxidation of the resulting trienyl sulfide to the corresponding sulfone. Total synthesis of lycopene starting from the C15 allylic sulfone 2b has been described, where the new C10 bis(chloroallylic) sulfone 11 proved to be a useful substitute for the C10 bis(chloroallylic) sulfide 3, which did not require the problematic chemoselective sulfur oxidation in a conjugated polyene.

A novel regioselective synthesis of allylsilanes

The anions derived from allyl sulfones were silylated in the α-position. Reductive desulfonylation gave the desired allylsilanes regioselectively