Ledol

Base Information

Chemical Name:Ledol
CAS No.:577-27-5
Molecular Formula:C15H26O
Molecular Weight:222.3663
Hs Code.:
DSSTox Substance ID:DTXSID40877915
Nikkaji Number:J21.647J
Wikipedia:Ledol
Wikidata:Q19291552
ChEMBL ID:CHEMBL4525000
Mol file:577-27-5.mol

Synonyms:ledol

Suppliers and Price of Ledol

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

American Custom Chemicals Corporation
LEDOL 95.00%
5MG
$ 496.73

Adipogen Life Sciences
Ledol ≥95%(NMR)
500 mg
$ 40.00

Total 8 raw suppliers

Chemical Property of Ledol

Chemical Property:

Vapor Pressure:0.000177mmHg at 25°C
Melting Point:104-105°
Refractive Index:nD110 1.4667
Boiling Point:293.9°Cat760mmHg
PKA:15.21±0.60(Predicted)
Flash Point:123.1°C
PSA：20.23000
Density:0.962g/cm³
LogP:3.46570
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:222.198365449
Heavy Atom Count:16
Complexity:309

Purity/Quality:

99% ^*data from raw suppliers

LEDOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2C1C3C(C3(C)C)CCC2(C)O
Isomeric SMILES:C[C@@H]1CC[C@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CC[C@@]2(C)O
Uses Ledol is an antifungal, toxic sesquiterpenoid, which exhibits expectorant and antitussive effects.

Technology Process of Ledol

There total 3 articles about Ledol 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:

: 25246-27-9
alloaromadendrene

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
ledol

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
(+)-viridiflorol

Guidance literature:: With lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) CHCl₃, RT, 30 min, 2.) Et₂O, RT, overnight;
DOI:10.1016/0040-4020(95)01079-3

Reference yield:

: 25246-27-9
alloaromadendrene

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
ledol

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
(+)-viridiflorol

Guidance literature:: With lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) CHCl₃, RT, 30 min, 2.) Et₂O, RT, overnight;
DOI:10.1016/0040-4020(95)01079-3