Alfadolone acetate

Base Information

Chemical Name:Alfadolone acetate
CAS No.:23930-37-2
Molecular Formula:C₂₃H₃₄O₅
Molecular Weight:390.52
Hs Code.:
European Community (EC) Number:245-942-5
UNII:00TN4GS00S
DSSTox Substance ID:DTXSID7045443
Nikkaji Number:J21.004H
Wikidata:Q27164650
NCI Thesaurus Code:C98249
Metabolomics Workbench ID:198440
ChEMBL ID:CHEMBL1874407
Mol file:23930-37-2.mol

Synonyms:21-acetoxy-3-alpha-hydroxy-5-alpha-pregnane-11,20-dione;alfadolone;alphadolone;alphadolone acetate;alphadolone, (3alpha,5beta)-isomer;alphadolone, (3beta,5alpha)-isomer

Suppliers and Price of Alfadolone acetate

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

Biosynth Carbosynth
3a,21-Dihydroxy-5a-pregnane-11,20-dione 21-acetate
10 mg
$ 400.00

Biosynth Carbosynth
3a,21-Dihydroxy-5a-pregnane-11,20-dione 21-acetate
1 mg
$ 80.00

American Custom Chemicals Corporation
ALFADOLONE ACETATE 95.00%
5MG
$ 501.55

Total 8 raw suppliers

Chemical Property of Alfadolone acetate

Chemical Property:

Melting Point:175-177°
Boiling Point:523.6°Cat760mmHg
PKA:15.04±0.70(Predicted)
Flash Point:175.1°C
PSA：80.67000
Density:1.164g/cm³
LogP:3.31740
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:390.24062418
Heavy Atom Count:28
Complexity:687

Purity/Quality:

97% ^*data from raw suppliers

3a,21-Dihydroxy-5a-pregnane-11,20-dione 21-acetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCC(=O)C1CCC2C1(CC(=O)C3C2CCC4C3(CCC(C4)O)C)C
Isomeric SMILES:CC(=O)OCC(=O)[C@H]1CC[C@@H]2[C@@]1(CC(=O)[C@H]3[C@H]2CC[C@@H]4[C@@]3(CC[C@H](C4)O)C)C

Technology Process of Alfadolone acetate

There total 5 articles about Alfadolone acetate 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: