Carvonecamphor

Base Information

Chemical Name:Carvonecamphor
CAS No.:39196-52-6
Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Hs Code.:
NSC Number:120530
DSSTox Substance ID:DTXSID50959973
Nikkaji Number:J55.633E

Synonyms:39196-52-6;NSC120530;SCHEMBL2386033;DTXSID50959973;NSC-120530;1,2-Dimethyltricyclo[3.3.0.0~2,7~]octan-3-one

Suppliers and Price of Carvonecamphor

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

Total 0 raw suppliers

Chemical Property of Carvonecamphor

Chemical Property:

Vapor Pressure:0.145mmHg at 25°C
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:258

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12CC3C1(C(=O)CC2C3)C

Technology Process of Carvonecamphor

There total 6 articles about Carvonecamphor 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: 94.4%

: 64-17-5
ethanol

: 2244-16-8,6485-40-1
(S)-p-mentha-6,8-dien-2-one

: 39196-52-6
Carvonecamphor

: 4638-90-8
1-exo,5-dimethyl-syn-2-<(ethoxycarbonyl)-methyl>bicyclo<2.1.1>hexane

Guidance literature:: at 26 ℃; Product distribution; Mechanism; Irradiation; another antipode; var. irradiation's sources;
DOI:10.1021/jo00137a017