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Methylstenbolone

Base Information Edit
  • Chemical Name:Methylstenbolone
  • CAS No.:6176-38-1
  • Molecular Formula:C21H32O2
  • Molecular Weight:316.484
  • Hs Code.:
  • NSC Number:74234
  • UNII:SE6T9C1YMB
  • DSSTox Substance ID:DTXSID301045943
  • Nikkaji Number:J2.791.532I
  • Wikipedia:Methylstenbolone
  • Wikidata:Q27148635
  • Mol file:6176-38-1.mol
Methylstenbolone

Synonyms:2,17-dimethyl-17-hydroxyandrost-1-en-3-one;2,17alpha-dimethyl-17beta-hydroxy-5alpha-androst-1-en-3-one;methylstenbolone

Suppliers and Price of Methylstenbolone
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
  • American Custom Chemicals Corporation
  • 2,17-ALPHA-DIMETHYL-17-BETA-HYDROXY-5-ALPHA-ANDROST-1-ENE-3-ONE 95.00%
  • 5MG
  • $ 499.63
Total 22 raw suppliers
Chemical Property of Methylstenbolone Edit
Chemical Property:
  • Vapor Pressure:2.58E-09mmHg at 25°C 
  • Refractive Index:1.533 
  • Boiling Point:433.018 °C at 760 mmHg 
  • Flash Point:184.694 °C 
  • PSA:37.30000 
  • Density:1.064 g/cm3 
  • LogP:4.51530 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:316.240230259
  • Heavy Atom Count:23
  • Complexity:578
Purity/Quality:

99% *data from raw suppliers

2,17-ALPHA-DIMETHYL-17-BETA-HYDROXY-5-ALPHA-ANDROST-1-ENE-3-ONE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC2(C(CCC3C2CCC4(C3CCC4(C)O)C)CC1=O)C
  • Isomeric SMILES:CC1=C[C@]2([C@@H](CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(C)O)C)CC1=O)C
  • Uses Methylstenbolone is an anabolic androgenic steroid that have been studied in respect of testosterone-receptor interaction and in the development of QSAR models.
Technology Process of Methylstenbolone

There total 3 articles about Methylstenbolone 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:
1.) Bromierung von 2α.17α-Dimethyl-androstanol-(17β)-on-(3), Eg., Na-Acetat 2.) HBr-Abspaltung in Dimethylacetamid, CaCO3, 30 Min., Kochen;
DOI:10.1021/ja01505a045
Guidance literature:
17α-Methyl-2-methylen-androstandiol-(3β,17β), Ggw. v. Pd 1) LiAlH4 ; Isolierung 2) 5,6-Dichlor-2,3-dicyan-benzochinon-(1,4) ; neben 2α,17α-Dimethyl-dihydrotestosteron;
DOI:10.1021/jm00338a020
Guidance literature:
Aus 17α-Methyldihydrotestosteron;
Refernces Edit
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