Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Epimethandienone

Base Information Edit
  • Chemical Name:Epimethandienone
  • CAS No.:33526-40-8
  • Molecular Formula:C20H28O2
  • Molecular Weight:300.43512
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00187168
  • Nikkaji Number:J393.536A
  • Wikidata:Q83058733
  • Mol file:33526-40-8.mol
Epimethandienone

Synonyms:Epimethandienone;17-Epimethandienone;33526-40-8;17-Epimethandrostenolone;SCHEMBL21177905;DTXSID00187168;Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17alpha)-;(8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one

Suppliers and Price of Epimethandienone
Supply Marketing:Edit
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
  • Usbiological
  • 17-Epimethandienone
  • 5mg
  • $ 460.00
Total 2 raw suppliers
Chemical Property of Epimethandienone Edit
Chemical Property:
  • Melting Point:161 - 163 °C 
  • PSA:37.30000 
  • LogP:4.04530 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:300.208930132
  • Heavy Atom Count:22
  • Complexity:589
Purity/Quality:

99% *data from raw suppliers

17-Epimethandienone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCC3C(C1CCC2(C)O)CCC4=CC(=O)C=CC34C
  • Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@]2(C)O)CCC4=CC(=O)C=C[C@]34C
  • Uses 17-Epimethandienone is an epimer of Methandrostenolone (M226000), an orally effective anabolic steroid.
Technology Process of Epimethandienone

There total 7 articles about Epimethandienone 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:
beim Behandeln den Extrakt in Ethylenchlorid von Produkten der Bakteriengaerung (Methylandrostenolon mit Cephalosporium C-9) mit β-Naphthol und anschliessend ausgeschiedenes Addukt mit wss.NaOH;
Guidance literature:
methylene chloride; With magnesium; In tetrahydrofuran; at 30 - 35 ℃;
androsta-1,4-diene-3,17-dione; In tetrahydrofuran; at 50 - 55 ℃; Temperature; Solvent;
Post RFQ for Price