56194-28-6

Basic information

• Product Name: 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol
• Synonyms: 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol
• CAS NO: 56194-28-6
• Molecular Weight: 222.371
• Mol File: 56194-28-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol(56194-28-6)
• EPA Substance Registry System: 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol(56194-28-6)

Safety Data

• Hazardous Substances Data: 56194-28-6(Hazardous Substances Data)

Upstream product

• 40716-66-3 (E)-3,7,11-trimethyl-1,6,10-dodecatrien-3-ol 

Downstream Products

• 24163-93-7 farnesyl bromide 
• 502-67-0 Farnesal 
• 4380-32-9 (2Z,6E)-farnesal 
• 4895-19-6 4-(4-methylphenyl)pentanal 
• 66958-32-5 1,4-Bis-benzyloxy-2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-29-(toluene-4-sulfonyl)-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methyl-benzene 
• 83626-16-8 Acetic acid 4-hydroxy-2,3,6-trimethyl-5-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-phenyl ester 
• 83626-17-9 Acetic acid 4-hydroxy-2,3,6-trimethyl-5-((2Z,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-phenyl ester 
• 1173-76-8 2,3-Dimethoxy-5-methyl-6-((2Z,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-[1,4]benzoquinone 
• 83626-21-5 2,3-Dimethoxy-6-methyl-4-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyloxy)-phenol 
• 83626-10-2 Acetic acid 2,3,6-trimethyl-4-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyloxy)-phenyl ester 
• 69422-80-6 2,3-Dimethoxy-5-methyl-6-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-benzene-1,4-diol 
• 1173-76-8 ubiquinone Q₃ 
• 74284-79-0 (6Z,8E,10E,14E,18E)-13-(Diphenyl-phosphinoyl)-2,6,10,15,19,23-hexamethyl-tetracosa-2,6,8,10,14,18,22-heptaen-12-ol 
• 74284-79-0 (6Z,8E,10E,14E,18E)-13-(Diphenyl-phosphinoyl)-2,6,10,15,19,23-hexamethyl-tetracosa-2,6,8,10,14,18,22-heptaen-12-ol 

Relevant articles and documents

CYCLIZATION OF SOME LINEAR TERPENOLS INITIATED BY "ACTIVATED" DMSO

It was shown that the acylhydroxysulfonium salt generated in situ from DMSO and trifluoroacetic anhydride causes low-temperature cyclization of geraniol, linalool, and nerol in an aprotic medium to a mixture of p-menthane monoterpenoids, and the maximum yield is obtained in the case of the last two terpenols.A similar result was obtained for E-nerolidol.