trans-Ocimenone

Base Information

Chemical Name:trans-Ocimenone
CAS No.:33746-72-4
Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Hs Code.:
DSSTox Substance ID:DTXSID601317761
Nikkaji Number:J2.305.228H
Wikidata:Q67879844
Mol file:33746-72-4.mol

Synonyms:trans-Ocimenone;(E)-Tagetenone;trans-Tagetenone;(e)-ocimenone;SCHEMBL2133996;(E)-Ocimenone (trans-ocimenone);XUINKEIPBTYUJP-VQHVLOKHSA-N;DTXSID601317761;(E)-2,6-Dimethylocta-2,5,7-trien-4-one;Q67879844

Suppliers and Price of trans-Ocimenone

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)-Ocimenone
100mg
$ 1320.00

TRC
(E)-Ocimenone
10 mg
$ 165.00

Medical Isotopes, Inc.
(E)-Ocimenone
100 mg
$ 2200.00

Total 4 raw suppliers

Chemical Property of trans-Ocimenone

Chemical Property:

PSA：17.07000
LogP:2.65400
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:215

Purity/Quality:

99% ^*data from raw suppliers

(E)-Ocimenone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CC(=O)C=C(C)C=C)C
Isomeric SMILES:CC(=CC(=O)/C=C(\C)/C=C)C
Uses (E)-Ocimenone, is the derivative of Ocimene (O150010), which are found in a variety of plants and fruits. The mixture of (E)-OciMenone, as well as its pure form, are oils with a pleasant odors, and thus can be used in perfumery Industry.

Technology Process of trans-Ocimenone

There total 15 articles about trans-Ocimenone 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: 63.0%