2,6,10-Trimethyl-2,6,10-dodecatrien-12-al

Base Information

• Chemical Name: 2,6,10-Trimethyl-2,6,10-dodecatrien-12-al
• CAS No.: 19317-11-4
• Molecular Formula: C15H24 O
• Molecular Weight: 220.355
• Hs Code.: 2912190090
• DSSTox Substance ID: DTXSID80862062
• Wikidata: Q27109827
• Mol file: 19317-11-4.mol

Synonyms:3,7,11-Trimethyl-dodeca-2,6,10-trienal;SCHEMBL379953;DTXSID80862062;FT-0626381;3,7,11-trimethyldodeca-2,6,10-trien-1-al;2,6,10-trimethyl-2,6,10-dodecatrien-12-al;Q27109827

Chemical Property of 2,6,10-Trimethyl-2,6,10-dodecatrien-12-al

Chemical Property:

• Vapor Pressure: 0.000187mmHg at 25°C
• Refractive Index: n20/D >1.4920(lit.)
• Boiling Point: 328.6°Cat760mmHg
• Flash Point: 147.8°C
• PSA: 17.07000
• Density: 0.868g/cm³
• LogP: 4.60450
• Storage Temp.: Amber Vial, Refrigerator
• Solubility.: Chloroform (Sparingly), Methanol (Sparingly)
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 220.182715385
• Heavy Atom Count: 16
• Complexity: 289

Purity/Quality:

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

Farnesone(MixtureofIsomers,TechnicalGrade) ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(=CCCC(=CCCC(=CC=O)C)C)C
• Uses: Farnesone is s useful building block for organic synthesis Farnesal was used in the synthesis of sesquiterpene nanaimoal.

Technology Process of 2,6,10-Trimethyl-2,6,10-dodecatrien-12-al

There total 22 articles about 2,6,10-Trimethyl-2,6,10-dodecatrien-12-al 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: 100.0%

farnesol (4602-84-0) → farnesal (19317-11-4)

Guidance literature:

With dipyridinium dichromate; In dichloromethane; at 0 - 25 ℃; for 24h;

DOI:10.1002/ejoc.200390189

Reference yield: 98.6%

3,7,11-trimethyl-6,10-dodecadien-1-yn-3-ol (2387-68-0,54325-12-1) → farnesal (19317-11-4)

Guidance literature:

With carbon dioxide; ruthenium-carbon composite; In ethanol; at 60 ℃; for 5h; under 750.075 Torr; Temperature; Solvent; Reagent/catalyst;

Reference yield: 66.0%

N-cyclohexyl-N-farnesylbenzenesulfinamide (78804-15-6) → farnesal (19317-11-4)

Guidance literature:

With potassium carbonate; In o-xylene; for 13h; Heating;

DOI:10.1021/jo00335a076

upstream raw materials:

pyridine

farnesyl bromide

chloroform

farnesol

Downstream raw materials:

pseudo-ionone

farnesol

4,8,12-trimethyl-1,3,7,11-tridecatetraene

(3E,7E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene

Refernces

• 1、 -. "ANTICANCER MICRORNA AND LIPID FORMULATIONS THEREOF". Paragraph 0347; 0349. . Retrieved 2021/02/12.
• 2、 -. "ADHESION PREVENTING AGENT". Paragraph 0368; 0369. . Retrieved 2016/04/20.