(-)-Epicedrol

Base Information

Chemical Name:(-)-Epicedrol
CAS No.:19903-73-2
Molecular Formula:C15H26 O
Molecular Weight:222.371
Hs Code.:
DSSTox Substance ID:DTXSID90425147
Nikkaji Number:J674.585G
Wikidata:Q27123312
Metabolomics Workbench ID:28415
Mol file:19903-73-2.mol

Synonyms:8-epicedrol;cedrol

Suppliers and Price of (-)-Epicedrol

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
Epicedrol
2.5mg
$ 150.00

TRC
Epicedrol
25mg
$ 1200.00

American Custom Chemicals Corporation
(-)-EPICEDROL 95.00%
5MG
$ 499.51

Total 4 raw suppliers

Chemical Property of (-)-Epicedrol

Chemical Property:

Vapor Pressure:0.000569mmHg at 25°C
Melting Point:36-39 °C
Refractive Index:1.519
Boiling Point:277.2°C at 760 mmHg
PKA:15.35±0.60(Predicted)
Flash Point:115.5°C
PSA：20.23000
Density:1g/cm³
LogP:3.60980
Storage Temp.:2-8°C
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:222.198365449
Heavy Atom Count:16
Complexity:321

Purity/Quality:

99% ^*data from raw suppliers

Epicedrol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2C13CCC(C(C3)C2(C)C)(C)O
Isomeric SMILES:C[C@@H]1CC[C@@H]2[C@]13CC[C@]([C@H](C3)C2(C)C)(C)O
General Description (-)-EPICEDROL is a sesquiterpene alcohol biosynthesized from (E,E)-farnesyldiphosphate (FPP) via the enzymatic action of epicedrol synthase. The hydroxyl group in its structure originates from water, as confirmed by isotopic labeling studies, rather than from the phosphate group of the substrate. This stereoselective cyclization results in a distinct molecular framework characterized by an octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-6-ol structure with a specific [3R-(3a,3ab,6b,7b,8aa)] configuration.

Technology Process of (-)-Epicedrol

There total 9 articles about (-)-Epicedrol 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: 69.0%

: 13567-54-9
cedrane

: 19903-73-2
(-)-(3R,3aS,6S,7R,8aS)-isocedrol

Guidance literature:: With ruthenium trichloride; sodium periodate; In tetrachloromethane; water; acetonitrile; at 25 ℃; for 30h;
DOI:10.1021/jo00046a040

Reference yield: 69.0%

: 10469-60-0,13567-54-9,13567-55-0,38227-41-7,38227-42-8,97305-23-2,97305-24-3
Cedrane

: 19903-73-2
epi-cedrol

Guidance literature:: With ruthenium trichloride; sodium periodate; In tetrachloromethane; water; acetonitrile; for 30h; Ambient temperature;
DOI:10.1016/S0040-4039(01)93761-X