Stemar-13-ene

Base Information

Chemical Name:Stemar-13-ene
CAS No.:138883-56-4
Molecular Formula:C₂₀H₃₂
Molecular Weight:272.474
Hs Code.:
DSSTox Substance ID:DTXSID501027117
Metabolomics Workbench ID:28501
Nikkaji Number:J748.297C
Wikidata:Q7607306
Wikipedia:Stemarene

Synonyms:stemar-13-ene

Suppliers and Price of Stemar-13-ene

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 0 raw suppliers

Chemical Property of Stemar-13-ene

Chemical Property:

XLogP3:6.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:272.250401021
Heavy Atom Count:20
Complexity:457

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC2CCC3C(CCCC3(C24CCC1C4)C)(C)C
Isomeric SMILES:CC1=C[C@@H]2CC[C@@H]3[C@@]([C@@]24CC[C@@H]1C4)(CCCC3(C)C)C

Technology Process of Stemar-13-ene

There total 10 articles about Stemar-13-ene 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: 96.0%

: 138922-83-5
13-Methyl-9β,13β-ethano-9β-podocarpan-12α-ol

: 138883-56-4
(+)-stemar-13-ene

Guidance literature:: With toluene-4-sulfonic acid; In benzene; for 3h; Heating;
DOI:10.1002/hlca.19910740807

Reference yield: 76.0%

: 1316759-88-2
C₂₂H₃₄S₂

: 138883-56-4
(+)-stemar-13-ene

Guidance literature:: With Raney-Ni; In ethanol; at 60 ℃; for 0.5h;
DOI:10.1021/jo200945s

Reference yield:

: C₂₉H₄₀O₂S₂

: 138883-56-4
(+)-stemar-13-ene

Guidance literature:: Multi-step reaction with 3 steps

1: Raney-Ni / Heating

2: 48 percent / LiAlH₄ / tetrahydrofuran / 0 °C

3: 96 percent / TsOH / benzene / 3 h / Heating

With lithium aluminium tetrahydride; toluene-4-sulfonic acid; nickel; In tetrahydrofuran; benzene;
DOI:10.1002/hlca.19910740807