Dihydrofarnesol

Base Information

Chemical Name:Dihydrofarnesol
CAS No.:51411-24-6
Molecular Formula:C₁₅H₂₈O
Molecular Weight:224.387
Hs Code.:
European Community (EC) Number:610-659-1
UNII:2U2PG80P22
Nikkaji Number:J639.422A,J104.557A
Wikidata:Q27255599
Metabolomics Workbench ID:3235
Mol file:51411-24-6.mol

Synonyms:2,3-dihydrofarnesol

Suppliers and Price of Dihydrofarnesol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(E)-3,7,11-Trimethyldodeca-6,10-dien-1-ol
250mg
$ 215.00

Total 18 raw suppliers

Chemical Property of Dihydrofarnesol

Chemical Property:

Vapor Pressure:6.5E-05mmHg at 25°C
Refractive Index:1.47
Boiling Point:307.8°C at 760 mmHg
PKA:15.12±0.10(Predicted)
Flash Point:104.9°C
PSA：20.23000
Density:0.86g/cm³
LogP:4.47780
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:5.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:224.214015512
Heavy Atom Count:16
Complexity:222

Purity/Quality:

99% ,98%,Electron Grade , ^*data from raw suppliers

(E)-3,7,11-Trimethyldodeca-6,10-dien-1-ol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Alcohols and Polyols, Other
Canonical SMILES:CC(CCC=C(C)CCC=C(C)C)CCO
Isomeric SMILES:CC(CC/C=C(\C)/CCC=C(C)C)CCO
Uses (E)-3,7,11-Trimethyldodeca-6,10-dien-1-ol dermatophytes inhibits the growth of dermatophytes.

Technology Process of Dihydrofarnesol

There total 24 articles about Dihydrofarnesol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 172376-82-8
(R)-2,3-dihydrofarnesal

: 20576-54-9,27745-36-4,37519-97-4,51411-24-6,69686-26-6,69743-81-3,76190-00-6,113889-56-8,34083-92-6
(3R)-(6E)-2,3-dihydrofarnesol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether;
DOI:10.1002/hlca.201300286

Reference yield: 96.0%

: 106-28-5
Farnesol

: 20576-54-9,34083-92-6,37519-97-4,51411-24-6,69686-26-6,69743-81-3,76190-00-6,113889-56-8,27745-36-4
(3S)-(6E)-2,3-dihydrofarnesol

Guidance literature:: With diacetato[(R)-(+)-2,2-bis(di-p-tolylphosphono)-1,1′?binaphthyl]ruthenium(II); hydrogen; In methanol; at 20 ℃; for 5h; under 26252.6 Torr; enantioselective reaction; High pressure; Autoclave;
DOI:10.1002/ejoc.201800199

Reference yield:

: 106-28-5
Farnesol

: 20576-54-9,27745-36-4,37519-97-4,51411-24-6,69686-26-6,69743-81-3,76190-00-6,113889-56-8,34083-92-6
(3R)-(6E)-2,3-dihydrofarnesol

: 20576-54-9,34083-92-6,37519-97-4,51411-24-6,69686-26-6,69743-81-3,76190-00-6,113889-56-8,27745-36-4
(3S)-(6E)-2,3-dihydrofarnesol

Guidance literature:: With chloro[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphytyl](p-cymene)ruthenium(II) chloride; potassium hydroxide; at 83 ℃; for 16h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201107910