13-Epitorulosol

Base Information

Chemical Name:13-Epitorulosol
CAS No.:3650-30-4
Molecular Formula:C₂₀H₃₄O₂
Molecular Weight:306.489
Hs Code.:
DSSTox Substance ID:DTXSID101110479
Nikkaji Number:J120.769E
Wikidata:Q105111935

Synonyms:3650-30-4;13-Epitorulosol;Epitorulosol;DTXSID101110479;(3S)-5-[(1S,4aR,5S,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol;(alphaS,1S,4aR,5S,8aR)-alpha-Ethenyldecahydro-5-(hydroxymethyl)-alpha,5,8a-trimethyl-2-methylene-1-naphthalenepropanol

Suppliers and Price of 13-Epitorulosol

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
LABD-8(17),14-dien-13,19-diol
5mg
$ 60.00

Total 4 raw suppliers

Chemical Property of 13-Epitorulosol

Chemical Property:

Vapor Pressure:2.12E-08mmHg at 25°C
Boiling Point:409.1°Cat760mmHg
Flash Point:176.3°C
PSA：40.46000
Density:0.99g/cm³
LogP:4.47480
XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:306.255880323
Heavy Atom Count:22
Complexity:443

Purity/Quality:

99% ^*data from raw suppliers

LABD-8(17),14-dien-13,19-diol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO
Isomeric SMILES:C[C@@]1(CCC[C@]2([C@H]1CCC(=C)[C@@H]2CC[C@@](C)(C=C)O)C)CO

Technology Process of 13-Epitorulosol

There total 3 articles about 13-Epitorulosol 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:

: 596-85-0
epimanool

: 1438-65-9,1908-44-7,3650-30-4,4549-12-6,33947-55-6,150134-40-0
labda-8(17),14-dien-13β,18-diol

Guidance literature:: Multi-step reaction with 2 steps

1: microbial transformation by Rhodococcus erythropolis JTS-131, 1.) (NH₄)2SO₄, K₂HPO₄, MgSO₄*7H₂O, CaCl₂*2H₂O, FeSO₄*7H₂O, Tween-60, 28 deg C, 12 h 2.) EDTA, 28 deg C, 48 h

2: LiAlH₄ / dioxane / 1 h / Heating

With lithium aluminium tetrahydride; In 1,4-dioxane;