17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate

Base Information

• Chemical Name: 17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate
• CAS No.: 13546-45-7
• Molecular Formula: C24H34O4S
• Molecular Weight: 418.5894
• UNII: UJ7V1I426A
• Nikkaji Number: J2.790.284G
• Wikidata: Q27148829
• Mol file: 13546-45-7.mol

Synonyms:UNII-UJ7V1I426A;UJ7V1I426A;17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate;NSC 72261;13546-45-7;NSC-72261;CHEBI:79698;Q27148829;17.BETA.-HYDROXY-4-MERCAPTOANDROST-4-EN-3-ONE 4-ACETATE 17-PROPIONATE;ANDROST-4-EN-3-ONE, 17.BETA.-HYDROXY-4-MERCAPTO-, 4-ACETATE 17-PROPIONATE;ACETIC ACID, THIO-, S-ESTER WITH 17.BETA.-HYDROXY-4-MERCAPTOANDROST-4-EN-3-ONE 17-PROPIONATE

Chemical Property of 17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate

Chemical Property:

• Vapor Pressure: 3.12E-11mmHg at 25°C
• Boiling Point: 527.9°Cat760mmHg
• Flash Point: 253.1°C
• Density: 1.18g/cm³
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 418.21778074
• Heavy Atom Count: 29
• Complexity: 771

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(=O)OC1CCC2C1(CCC3C2CCC4=C(C(=O)CCC34C)SC(=O)C)C
• Isomeric SMILES: CCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C(C(=O)CC[C@]34C)SC(=O)C)C

Technology Process of 17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate

There total 2 articles about 17beta-Hydroxy-4-mercaptoandrost-4-en-3-one 4-acetate 17-propionate 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:

→ 4-(Acetylthio)-testosteron-propionat (13546-45-7)

Guidance literature:

Testosteron-propionat-4β,5β-epoxid, Thioessigsaeure;

Reference yield:

→ 4-Acetylmercapto-testosteron-propionat (13546-45-7)

Guidance literature:

4-Acetylmercapto-testosteron, Propionsaeure-anhydrid/Py., 20grad, 12h;