Cinnamolide

Base Information

Chemical Name:Cinnamolide
CAS No.:23599-47-5
Molecular Formula:C15H22O2
Molecular Weight:234.33
Hs Code.:
ChEMBL ID:CHEMBL218666
DSSTox Substance ID:DTXSID201339979
Metabolomics Workbench ID:114504
Nikkaji Number:J16.590E
Wikidata:Q77368606
Mol file:23599-47-5.mol

Synonyms:Cinnamolide;23599-47-5;(5aS,9aS,9bR)-6,6,9a-trimethyl-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-3-one;(-)-Cinnamolide;CHEMBL218666;CHEBI:202004;DTXSID201339979;BDBM50465349;AKOS040762611;Naphtho(1,2-c)furan-3(1H)-one, 5,5a,6,7,8,9,9a,9b-octahydro-6,6,9a-trimethyl-, (5aS-(5a-alpha,9a-beta,9b-alpha))-;(5aS,9aS,9bR)-6,6,9a-trimethyl-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzouran-3-one;(5aS,9aS,9bR)-6,6,9a-trimethyl-5,5a,7,8,9,9b-hexahydro-1H-benzo[e]isobenzofuran-3-one;(5aS)-6,6,9a|A-Trimethyl-5,5a|A,6,7,8,9,9a,9b|A-octahydronaphtho[1,2-c]furan-3(1H)-one;(5aS, 9aS, 9bR)-6, 6, 9a-trimethyl-5, 5a, 7, 8, 9, 9b-hexahydro-1H-benzo[e][2]benzofuran-3-one

Suppliers and Price of Cinnamolide

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 3 raw suppliers

Chemical Property of Cinnamolide

Chemical Property:

Melting Point:125-126 °C
Boiling Point:363.9±11.0 °C(Predicted)
PSA：26.30000
Density:1.07±0.1 g/cm3(Predicted)
LogP:3.32210
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:234.161979940
Heavy Atom Count:17
Complexity:394

Purity/Quality:: 98.0% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(CCCC2(C1CC=C3C2COC3=O)C)C
Isomeric SMILES:C[C@]12CCCC([C@@H]1CC=C3[C@@H]2COC3=O)(C)C

Technology Process of Cinnamolide

There total 12 articles about Cinnamolide 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%

: 22567-27-7,34437-62-2,79732-75-5,90581-65-0,94942-39-9,106622-50-8,146276-81-5
(4aRS,5SR,8aRS)-<1,2,3,4,5,8,8a-octahydro-6-(hydroxymethyl)-1,1,4a-trimethylnaphthalen-5-yl>methanol

: 23599-47-5,28400-16-0
cinnamolide

Guidance literature:: With silver carbonate; In benzene; for 1.5h; Heating;

Reference yield: 88.0%

: 34437-62-2
drimendiol

: 28400-16-0,23599-47-5
cinnamolide

Guidance literature:: With manganese(IV) oxide; In dichloromethane; for 48h;
DOI:10.1021/acs.jnatprod.6b01056

Reference yield: 80.0%

: dithiocarbonic acid O-(2,2-dimethyl-propyl) ester S-(6,6,9a-trimethyl-3-oxo-dodecahydro-naphtho[1,2-c]furan-4-yl) ester

: 23599-47-5,28400-16-0
cinnamolide

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In chloroform; for 0.25h; Ambient temperature;
DOI:10.1016/S0040-4020(98)01184-3