7-beta-Hydroxyepiandrosterone

Base Information

Chemical Name:7-beta-Hydroxyepiandrosterone
CAS No.:25848-69-5
Molecular Formula:C₁₉H₃₀O₃
Molecular Weight:306.445
Hs Code.:
UNII:OCP3E5KD08
DSSTox Substance ID:DTXSID701293235
Nikkaji Number:J1.834.869A
Wikipedia:7%CE%B2-Hydroxyepiandrosterone
Wikidata:Q27896214
Metabolomics Workbench ID:149864

Synonyms:7-hydroxyandrosterone;7-OH-EPIA;7beta-hydroxy-epiandrosterone

Suppliers and Price of 7-beta-Hydroxyepiandrosterone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 7-beta-Hydroxyepiandrosterone

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:306.21949481
Heavy Atom Count:22
Complexity:489

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O
Isomeric SMILES:C[C@]12CC[C@@H](C[C@@H]1C[C@@H]([C@@H]3[C@@H]2CC[C@]4([C@H]3CCC4=O)C)O)O
Recent ClinicalTrials:European Study of HF0220 in Mild to Moderate Alzheimer's Disease Patients
Recent EU Clinical Trials:Chemical Safety/Tolerability of HF0220 and its Effect on Biochemical Markers Relevant to Patients with a Diagnosis of Mild to Moderate Alzheimer's Disease.

Technology Process of 7-beta-Hydroxyepiandrosterone

There total 6 articles about 7-beta-Hydroxyepiandrosterone 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: 3.0%

: 1239-31-2
3β-acetoxy-5α-androstan-17-one

: 25848-68-4
3beta-7alpha-Dihydroxy-5alpha-androstane-17-one

: 25848-69-5
3beta-7beta-Dihydroxy-5alpha-androstane-17-one

: 49643-99-4
3beta-hydroxy-5alpha-Androstane-7,17-dione

Guidance literature:: In ethanol; at 25 ℃; for 72h; Cunninghamella elegans;
DOI:10.1039/P19810001041

Reference yield: 2.0%

: 481-29-8
Epiandrosterone

: 58-22-0
testosterone

: 25848-75-3
3β,11α-dihydroxy-5α-androstan-17-one

: 25848-68-4
3beta-7alpha-Dihydroxy-5alpha-androstane-17-one

: 25848-69-5
3beta-7beta-Dihydroxy-5alpha-androstane-17-one

: 2260-01-7
1α,3β-dihydroxy-5α-androstan-17-one

: 897-06-3
Androsta-1,4-diene-3,17-dione

: 846-48-0,361432-76-0
1-dehydrotestosterone

: 62-99-7,2944-87-8,34096-63-4,34442-08-5,145772-79-8
6β-hydroxytestosterone

: 571-40-4
5α-androst-1-ene-3,17-dione

: 63-00-3
6β-hydroxy-4-androstene-3,17-dione

Guidance literature:: With malt extract; disodium hydrogenphosphate; calcium(II) chloride dihydrate; magnesium(II) chloride hexahydrate; strontium (III) chloride hexahydrate; potassium chloride; boric acid; sodium hydrogencarbonate; sodium sulfate; sodium chloride; potassium bromide; potassium hydroxide; In water; N,N-dimethyl-formamide; at 32 ℃; for 168h; pH=8; Enzymatic reaction;
DOI:10.3184/174751916X14786062524888