Aldosterone, monoacetate

Base Information

Chemical Name:Aldosterone, monoacetate
CAS No.:297-91-6
Molecular Formula:C23H30 O6
Molecular Weight:402.488
Hs Code.:
NSC Number:73857
UNII:RH7JOB7P70
DSSTox Substance ID:DTXSID701043375
Nikkaji Number:J82.261B
Wikidata:Q27288120
Mol file:297-91-6.mol

Synonyms:aldosterone-21-acetate;aldosterone-21-acetate, (+-)-isomer

Suppliers and Price of Aldosterone, monoacetate

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

American Custom Chemicals Corporation
11-BETA,18-EPOXY-18-HYDROXY-3,20-DIOXOPREGN-4-EN-21-YL ACETATE 95.00%
5MG
$ 504.92

Total 9 raw suppliers

Chemical Property of Aldosterone, monoacetate

Chemical Property:

Boiling Point:577.6°Cat760mmHg
Flash Point:197.5°C
PSA：97.74000
Density:1.26g/cm³
LogP:2.41650
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:402.20423867
Heavy Atom Count:29
Complexity:784

Purity/Quality:

99% ^*data from raw suppliers

11-BETA,18-EPOXY-18-HYDROXY-3,20-DIOXOPREGN-4-EN-21-YL ACETATE 95.00% ^*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(C3C2CCC4=CC(=O)CCC34C)O)C=O
Isomeric SMILES:CC(=O)OCC(=O)[C@H]1CC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)O)C=O

Technology Process of Aldosterone, monoacetate

There total 6 articles about Aldosterone, monoacetate 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:

: 297-91-6,1509-18-8
rac-21-acetoxy-11β-hydroxy-3,20-dioxo-pregn-4-en-18-al

: 297-91-6,1509-18-8
rac-21-acetoxy-11β-hydroxy-3,20-dioxo-17βH-pregn-4-en-18-al

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous methanol. K₂CO₃

2: durch aufeinanderfolgende Umsetzung mit wss. Essigsaeure

With potassium carbonate;
DOI:10.1002/hlca.19570400729