(3beta)-3,25-Dihydroxycholest-5-en-7-one

Base Information

• Chemical Name: (3beta)-3,25-Dihydroxycholest-5-en-7-one
• CAS No.: 64907-23-9
• Molecular Formula: C₂₇H₄₄O₃
• Molecular Weight: 416.645
• DSSTox Substance ID: DTXSID801308740
• Nikkaji Number: J3.387.440E
• Metabolomics Workbench ID: 156712
• ChEMBL ID: CHEMBL3311218

Synonyms:(3beta)-3,25-Dihydroxycholest-5-en-7-one;64907-23-9;7-keto-25-hydroxycholesterol;CHEMBL3311218;(3S,8S,9S,10R,13R,14S,17R)-3-hydroxy-17-[(2R)-6-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one;7-oxo-25-hydroxycholesterol;25-hydroxy 7-keto cholesterol;SCHEMBL2488125;CHEBI:180497;DTXSID801308740;BDBM50045537;PD088791

Chemical Property of (3beta)-3,25-Dihydroxycholest-5-en-7-one

Chemical Property:

• XLogP3: 5.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 416.32904526
• Heavy Atom Count: 30
• Complexity: 709

Purity/Quality:

≥95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(CCCC(C)(C)O)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C
• Isomeric SMILES: C[C@H](CCCC(C)(C)O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C(=O)C=C4[C@@]3(CC[C@@H](C4)O)C)C

Technology Process of (3beta)-3,25-Dihydroxycholest-5-en-7-one

There total 1 articles about (3beta)-3,25-Dihydroxycholest-5-en-7-one 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: 59.9%

25-hydroxychlolesterol (2140-46-7) → 7-oxo-cholest-5-ene-3β,25-diol (64907-23-9)

Guidance literature:

With tert.-butylhydroperoxide; N-hydroxyphthalimide; cobalt(II) acetate; In acetone; at 20 ℃; for 12h; regioselective reaction;

DOI:10.1016/j.steroids.2014.12.004

upstream raw materials:

25-hydroxychlolesterol

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