(2Z,6E)-Farnesyl acetate

Base Information

• Chemical Name: (2Z,6E)-Farnesyl acetate
• CAS No.: 40266-29-3
• Molecular Formula: C17H28O2
• Molecular Weight: 264.408
• UNII: 24D243N5BV
• Nikkaji Number: J674.468K
• Wikidata: Q27253842
• Mol file: 40266-29-3.mol

Synonyms:(2Z,6E)-Farnesyl acetate;(Z,E)-farnesyl acetate;Farnesyl acetate, (2Z,6E)-;cis-2-trans-6-Farnesyl acetate;(Z)-Farnesyl acetate;24D243N5BV;UNII-24D243N5BV;FEMA No. 4213, (2Z,6E)-;40266-29-3;2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, 1-acetate, (2Z,6E)-;cis-trans-Farnesyl acetate;SCHEMBL806690;Q27253842;(2Z,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol acetate

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

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

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

Guidance literature:

Brom-dodecatrien (II), KOCOCH3;

Reference yield:

acetic anhydride (108-24-7) + [(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate (40266-29-3) → C16H26 + C15H24 + (+/-)-cedrene (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) + epizonarene (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)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 0 ℃; for 120h; Inert atmosphere;

DOI:10.1002/anie.201906753

Reference yield:

[(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate (40266-29-3) → C16H26 + C15H24 + (+/-)-cedrene (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) + epizonarene (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)

Guidance literature:

With hydrogenchloride; C-undecylcalix[4]resorcinarene; In chloroform; at 30 ℃; for 120h; Temperature; Kinetics;

DOI:10.1002/anie.201906753

Downstream raw materials:

(+/-)-cedrene

epizonarene