Avocadene

Base Information

Chemical Name:Avocadene
CAS No.:83797-45-9
Molecular Formula:C₁₇H₃₄O₃
Molecular Weight:286.455
Hs Code.:
DSSTox Substance ID:DTXSID001003849
Nikkaji Number:J322.794D
Wikidata:Q82998554
Metabolomics Workbench ID:44669
ChEMBL ID:CHEMBL480091

Synonyms:avocadene

Suppliers and Price of Avocadene

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
rac-Avocadene
25mg
$ 410.00

Total 3 raw suppliers

Chemical Property of Avocadene

Chemical Property:

Vapor Pressure:1.84E-09mmHg at 25°C
Boiling Point:436.8°Cat760mmHg
Flash Point:194.2°C
PSA：60.69000
Density:0.962g/cm³
LogP:3.56770
XLogP3:4.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:15
Exact Mass:286.25079494
Heavy Atom Count:20
Complexity:206

Purity/Quality:

99% ^*data from raw suppliers

rac-Avocadene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCCCCCCCCCCCC(CC(CO)O)O

Technology Process of Avocadene

There total 4 articles about Avocadene 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:

: 24607-05-4,34524-38-4
avocadyne

: 83797-45-9
1,2,4-trihydroxy-heptadeca-16-ene

Guidance literature:: With hydrogen; Pd-BaSO₄; In pyridine;
DOI:10.1016/S0040-4020(01)83005-2

Reference yield:

: 24607-06-5
avocadyne acetate

: 83797-45-9
1,2,4-trihydroxy-heptadeca-16-ene

Guidance literature:: Multi-step reaction with 2 steps

1: MeOH, HCl

2: H₂ / Pd/BaSO₄ / pyridine

With hydrogenchloride; methanol; hydrogen; Pd-BaSO₄; In pyridine;
DOI:10.1016/S0040-4020(01)83005-2