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Epiyohimbol

Base Information
  • Chemical Name:Epiyohimbol
  • CAS No.:439-70-3
  • Molecular Formula:C19H24N2O
  • Molecular Weight:296.41
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40963140
  • Nikkaji Number:J13.472D
  • Wikidata:Q27116537
  • Metabolomics Workbench ID:55167
  • ChEMBL ID:CHEMBL4080585
  • Mol file:439-70-3.mol
Epiyohimbol

Synonyms:Epiyohimbol;17beta-yohimbol;439-70-3;17-beta-Yohimbol;yohimban-17beta-ol;Yohimban-17-beta-ol;Yohimban-17-ol, (17-beta)-;(1S,15R,18R,20R)-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-18-ol;CHEMBL4080585;CHEBI:35635;DTXSID40963140;LS-162760;Q27116537

Suppliers and Price of Epiyohimbol
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
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Total 0 raw suppliers
Chemical Property of Epiyohimbol
Chemical Property:
  • Vapor Pressure:7.84E-11mmHg at 25°C 
  • Boiling Point:500.4°C at 760 mmHg 
  • Flash Point:256.4°C 
  • PSA:68.15000 
  • Density:1.27g/cm3 
  • LogP:-0.78400 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:296.188863393
  • Heavy Atom Count:22
  • Complexity:428
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2CN3CCC4=C(C3CC2CC1O)NC5=CC=CC=C45
  • Isomeric SMILES:C1C[C@H]2CN3CCC4=C([C@@H]3C[C@@H]2C[C@@H]1O)NC5=CC=CC=C45
Technology Process of Epiyohimbol

There total 10 articles about Epiyohimbol 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:
Guidance literature:
With tetrahydrofuran; lithium aluminium tetrahydride;
DOI:10.1002/hlca.19570400626 DOI:10.1021/ja01540a027
Guidance literature:
With lithium aluminium tetrahydride; diethyl ether; 3β-yohimban-17ξ-ol, whose methochloride by/at 278 degree is melting; Isolierung als Methochlorid;
DOI:10.1002/hlca.19570400626
Guidance literature:
With lithium aluminium tetrahydride; diethyl ether; ent-15β-yohimban-17ξ-ol, whose methopicrate by/at 222 degree is melting;
DOI:10.1002/hlca.19570400626
upstream raw materials:

yohimban-17-one

yohimban-17-one

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