Penmesterol

Base Information

• Chemical Name: Penmesterol
• CAS No.: 67-81-2
• Molecular Formula: C25H38O2
• Molecular Weight: 370.576
• European Community (EC) Number: 200-670-6
• UNII: D5F29U03HM
• ChEMBL ID: CHEMBL2104849
• DSSTox Substance ID: DTXSID301018944
• NCI Thesaurus Code: C170308
• Nikkaji Number: J4.853D
• Wikidata: Q15633969
• Wikipedia: Penmesterol
• Mol file: 67-81-2.mol

Synonyms:PENMESTEROL;67-81-2;Penmesterol [INN:DCF];RP 12222;D5F29U03HM;Pandrocine;RP-12222;Penmesterolo;Penmesterolum;Penmestrol;(8R,9S,10R,13S,14S,17S)-3-cyclopentyloxy-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-ol;Penmesterolo [DCIT];Penmesterolum [INN-Latin];UNII-D5F29U03HM;EINECS 200-670-6;PENMESTEROL [INN];17alpha-Methyltestosterone 3-cyclopentyl enol ether;SCHEMBL547668;CHEMBL2104849;CHEBI:135567;ZUBDXGHKAAMAAA-RFXJPFPRSA-N;DTXSID301018944;(10R,13S,17S)-3-Cyclopentyloxy-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta(a)phenanthren-17-ol;NS00041188;Q15633969;3-(Cyclopentyloxy)-17-methyl-androsta-3,5-dien-17beta-ol;17.ALPHA.-METHYLTESTOSTERONE 3-CYCLOPENTYL ENOL ETHER [MI];3-(CYCLOPENTYLOXY)-17-METHYL-ANDROSTA-3,5-DIEN-17.BETA.-OL

Chemical Property of Penmesterol

Chemical Property:

• Vapor Pressure: 1.69E-12mmHg at 25°C
• Melting Point: 162-168oC(lit.)
• Refractive Index: 1.565
• Boiling Point: 509.2 °C at 760 mmHg
• Flash Point: 219.6 °C
• PSA: 29.46000
• Density: 1.09 g/cm³
• LogP: 6.15320
• Solubility.: H2O: ≤0.5 mg/mL
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 370.287180451
• Heavy Atom Count: 27
• Complexity: 672

Purity/Quality:

99% ^*data from raw suppliers

Methyltestosterone United States Pharmacopeia (USP) Reference Standard ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 45-63
• Safety Statements: 53-36/37-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC(=CC1=CCC3C2CCC4(C3CCC4(C)O)C)OC5CCCC5
• Isomeric SMILES: C[C@]12CCC(=CC1=CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(C)O)C)OC5CCCC5
• Therapeutic Function: Androgen

Technology Process of Penmesterol

There total 1 articles about Penmesterol 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:

→ 3-Cyclopentyloxy-17α-methyl-androsta-3,5-dien-17β-ol (67-81-2)

Guidance literature:

entspr. Enolaether, MeMgBr;