Nandrolone cyclohexanecarboxylate

Base Information

• Chemical Name: Nandrolone cyclohexanecarboxylate
• CAS No.: 18470-94-5
• Molecular Formula: C25H36O3
• Molecular Weight: 384.559
• European Community (EC) Number: 242-351-4
• UNII: 45FAH33FMM
• DSSTox Substance ID: DTXSID10939877
• Nikkaji Number: J21.673I
• Wikipedia: Nandrolone_cyclohexanecarboxylate
• Wikidata: Q27258836
• Mol file: 18470-94-5.mol

Synonyms:Nandrolone cyclohexanecarboxylate;18470-94-5;Nor-durandron;17beta-Hydroxyestr-4-en-3-one 17-(cyclohexanecarboxylate);UNII-45FAH33FMM;45FAH33FMM;EINECS 242-351-4;[(8R,9S,10R,13S,14S,17S)-13-methyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl] cyclohexanecarboxylate;NOLONGANDRON;SCHEMBL604997;DTXSID10939877;NANDROLONE HEXAHYDROBENZOATE;19-nortestosterone cyclohexanecarboxylate;NANDROLONE CYCLOHEXANECARBOXYLATE [MI];Q27258836;Estr-4-en-3-one, 17-((cyclohexylcarbonyl)oxy)-, (17beta)-;ESTR-4-EN-3-ONE, 17-((CYCLOHEXYLCARBONYL)OXY)-, (17.BETA.)-

Chemical Property of Nandrolone cyclohexanecarboxylate

Chemical Property:

• Melting Point: 88-89°
• Boiling Point: 514.4°Cat760mmHg
• Flash Point: 221.3°C
• PSA: 43.37000
• Density: 1.12g/cm³
• LogP: 5.62030
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 384.26644501
• Heavy Atom Count: 28
• Complexity: 673

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC3C(C1CCC2OC(=O)C4CCCCC4)CCC5=CC(=O)CCC35
• Isomeric SMILES: C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OC(=O)C4CCCCC4)CCC5=CC(=O)CC[C@H]35

Technology Process of Nandrolone cyclohexanecarboxylate

There total 3 articles about Nandrolone cyclohexanecarboxylate 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-methoxy-17-hydroxyestra-2,5(10)-diene (1091-93-6) → 17β-cyclohexanecarbonyloxy-estr-4-en-3-one (18470-94-5)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous HCl

With hydrogenchloride;

DOI:10.1021/ja01602a054

Reference yield:

19-nortestosterone (434-22-0) → 17β-cyclohexanecarbonyloxy-estr-4-en-3-one (18470-94-5)

Guidance literature:

DOI:10.1021/ja01602a054

Reference yield:

→ Cyclohexanecarboxylic acid (13S,17S)-13-methyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester (18470-94-5)

Guidance literature:

19-Nor-testosteron, Hexahydrobenzoyl chlorid in Py;

upstream raw materials:

19-nortestosterone

3-methoxy-17-hydroxyestra-2,5⁽¹⁰⁾-diene

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