(+)-Chrysanthenone

Base Information

Chemical Name:(+)-Chrysanthenone
CAS No.:38301-80-3
Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Hs Code.:
UNII:5706LMQ84R,841NXH6XEV
DSSTox Substance ID:DTXSID801221097
Nikkaji Number:J1.245.910F
Wikidata:Q105969941
Wikipedia:Chrysanthenone

Synonyms:chrysanthenone

Suppliers and Price of (+)-Chrysanthenone

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 1 raw suppliers

Chemical Property of (+)-Chrysanthenone

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:248

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CCC2C(=O)C1C2(C)C
Isomeric SMILES:CC1=CC[C@H]2C(=O)[C@@H]1C2(C)C

Technology Process of (+)-Chrysanthenone

There total 2 articles about (+)-Chrysanthenone 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: 7.0%

: 58558-13-7
(2E)-3,7-dimethyl-2,6-octadienoyl chloride

: 473-06-3,38301-80-3,58437-73-3,97169-74-9
chrysanthenone

: 56001-54-8
6-(1-chloro-1-methylethyl)-3-methyl-2-cyclohexen-1-one

: 107514-23-8
7,7-dimethyl-2-methylenebicyclo<3.1.1>heptan-6-one

Guidance literature:: With triethylamine; In toluene; for 3h; Heating;
DOI:10.1021/jo00384a035

Reference yield:

: 4698-08-2
(E)-geranic acid

: 473-06-3,38301-80-3,58437-73-3,97169-74-9
chrysanthenone

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride / benzene / a) 25 deg C, 2 h, b) 45 deg C, 30 min

2: 2 percent / Et₃N / toluene / 3 h / Heating

With oxalyl dichloride; triethylamine; In toluene; benzene;
DOI:10.1021/jo00384a035