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11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone

Base Information
  • Chemical Name:11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone
  • CAS No.:124251-90-7
  • Molecular Formula:C20H24O5
  • Molecular Weight:344.408
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70924764
  • Mol file:124251-90-7.mol
11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone

Synonyms:11,18-epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone;6-hydroxyaldosterone-gamma-lactone;6-OH-aldosterone-lactone

Suppliers and Price of 11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone
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 3 raw suppliers
Chemical Property of 11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone
Chemical Property:
  • Vapor Pressure:1.6E-16mmHg at 25°C 
  • Boiling Point:592.8°Cat760mmHg 
  • PKA:13.95±0.40(Predicted) 
  • Flash Point:215.5°C 
  • PSA:83.83000 
  • Density:1.38g/cm3 
  • LogP:1.95470 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:344.16237386
  • Heavy Atom Count:25
  • Complexity:724
Purity/Quality:

98%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12C=CC(=O)C=C1C(CC3C2C4CC5(C3CCC5C(=O)O)CO4)O
  • Isomeric SMILES:C[C@]12C=CC(=O)C=C1[C@@H](C[C@@H]3[C@@H]2[C@@H]4CC5([C@H]3CC[C@@H]5C(=O)O)CO4)O
Technology Process of 11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone

There total 2 articles about 11,18-Epoxy-6-hydroxy-3-oxoandrost-4-ene-17,18-carbolactone 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:
Guidance literature:
With sodium hydroxide; iodosylbenzene; In 1,4-dioxane; for 12h;
DOI:10.1016/0039-128X(89)90092-5
Guidance literature:
Multi-step reaction with 2 steps
1: 67.3 mg / 60percent HClO4 / ethyl acetate / 0.5 h
2: 18 mg / iodosobenzene, aq. NaOH / dioxane / 12 h
With sodium hydroxide; perchloric acid; iodosylbenzene; In 1,4-dioxane; ethyl acetate;
DOI:10.1016/0039-128X(89)90092-5
upstream raw materials:

aldosterone γ-lactone

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