(2E,6Z)-farnesol acetate

Base Information

Chemical Name:(2E,6Z)-farnesol acetate
CAS No.:24163-98-2
Molecular Formula:C17H28O2
Molecular Weight:264.408
Hs Code.:
UNII:M3CY8SFI62
Wikidata:Q27283432
Mol file:24163-98-2.mol

Synonyms:(2E,6Z)-Farnesyl Acetate;(2E,6Z)-farnesol acetate;M3CY8SFI62;Farnesyl acetate, (2E,6Z)-;trans-2-cis-6-farnesyl acetate;UNII-M3CY8SFI62;FEMA No. 4213, (2E,6Z)-;24163-98-2;2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, acetate, (E,Z)-;2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, 1-acetate, (2E,6Z)-;(E,Z)-farnesyl acetate;SCHEMBL806725;Q27283432

Suppliers and Price of (2E,6Z)-farnesol acetate

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
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price

Total 0 raw suppliers

Chemical Property of (2E,6Z)-farnesol acetate

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:9
Exact Mass:264.208930132
Heavy Atom Count:19
Complexity:356

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C
Isomeric SMILES:CC(=CCC/C(=C\CC/C(=C/COC(=O)C)/C)/C)C

Technology Process of (2E,6Z)-farnesol acetate

There total 1 articles about (2E,6Z)-farnesol acetate 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:

: 4128-17-0,24163-97-1,24163-98-2,29548-30-9,40266-29-3
Acetic acid (2E,6Z)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester

Guidance literature:: Brom-dodecatrien (II), KOCOCH3;

Reference yield:

: 108-24-7
acetic anhydride

: 24163-98-2
3,7,11-trimethyl-2E,6Z,10-dodecatrienyl ethanoate

: 28624-23-9,28624-28-4,62358-43-4,473-14-3
2,3,4,4a,5,6-hexahydro-1,4a-dimethyl-7-(1-methylethyl)-naphthalene

: C₁₆H₂₆

: C₁₅H₂₄

: 469-61-4,19069-48-8,22567-43-7,35944-22-0,35964-52-4,37720-32-4,38227-40-6,50894-66-1,65354-33-8,65981-45-5
(+/-)-cedrene

: 5975-30-4,35938-51-3,36437-95-3,41702-63-0,41702-64-1,41929-05-9,51819-91-1,74036-35-4,76898-68-5,149115-45-7
epizonarene

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 ℃; for 192h; Inert atmosphere;
DOI:10.1002/anie.201906753

Reference yield:

: 24163-98-2
3,7,11-trimethyl-2E,6Z,10-dodecatrienyl ethanoate

: C₂₅H₃₆Br₂O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: bromodiethylsulfonium bromopentachloroantimonate / nitromethane / 0.01 h / 0 °C / Inert atmosphere

1.2: 1 h / 25 °C

2.1: thionyl chloride; triethylamine / dichloromethane / 0.5 h / -97 °C / Inert atmosphere

3.1: potassium carbonate; methanol / 1 h / 50 °C / Inert atmosphere

3.2: 25 °C / Cooling with ice

4.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 1 h / 0 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran; hexanes / 0.33 h / -78 °C / Inert atmosphere

5.2: 0.33 h / -40 °C / Inert atmosphere

With methanol; n-butyllithium; thionyl chloride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; triethylamine; bromodiethylsulfonium bromopentachloroantimonate; In tetrahydrofuran; hexanes; nitromethane; dichloromethane;