Methasterone

Base Information

• Chemical Name: Methasterone
• CAS No.: 3381-88-2
• Molecular Formula: C₂₁H₃₄O₂
• Molecular Weight: 318.5
• NSC Number: 40490
• UNII: GH88DY98MR
• DSSTox Substance ID: DTXSID10187472
• Nikkaji Number: J2.389.967A
• Wikipedia: Methasterone
• Wikidata: Q15409388
• Metabolomics Workbench ID: 199222
• Mol file: 3381-88-2.mol

Synonyms:2 alpha,17 alpha-dimethyldihydrotestosterone;2,17-dimethyldihydrotestosterone

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Chemical Property of Methasterone

Chemical Property:

• Vapor Pressure: 5.89E-09mmHg at 25°C
• Melting Point: 223-225℃
• Refractive Index: 1.518
• Boiling Point: 423.8 °C at 760 mmHg
• PKA: 15.15±0.70(Predicted)
• Flash Point: 180.8 °C
• PSA: 37.30000
• Density: 1.04 g/cm³
• LogP: 4.59520
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 318.255880323
• Heavy Atom Count: 23
• Complexity: 528

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1CC2(C(CCC3C2CCC4(C3CCC4(C)O)C)CC1=O)C
• Isomeric SMILES: C[C@@H]1C[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: Methasterone is an anabolic androgenic steroid. Methasterone is one of the anabolic steroids screened by the World Anti-Doping Agency (WADA).

Technology Process of Methasterone

There total 4 articles about Methasterone 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:

→ 2α,17α-Dimethyl-androstan-17β-ol-3-on (3381-88-2,88979-44-6,88979-48-0,110769-76-1)

Guidance literature:

Kat. Red. des entspr. 4-Androsten V;

Reference yield:

→ 2α,17α-Dimethyl-17β-hydroxy-5α-androstanon-(3) (3381-88-2,88979-44-6,88979-48-0,110769-76-1)

Guidance literature:

2α,17α-Dimethyl-testosteron, Li, fl. NH3, Ae., THF;

Reference yield:

→ (2R,17S)-17-Hydroxy-2,10,13,17-tetramethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one (3381-88-2,88979-44-6,88979-48-0,110769-76-1)

Guidance literature:

2α,17α-Dimethyltestosteron, Li-NH3(fl.);

Refernces