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6beta,19-Epoxypregn-4-ene-3,20-dione

Base Information
  • Chemical Name:6beta,19-Epoxypregn-4-ene-3,20-dione
  • CAS No.:2205-86-9
  • Molecular Formula:C21H28O3
  • Molecular Weight:328.452
  • Hs Code.:
  • Nikkaji Number:J662.262C
  • Wikidata:Q27148770
6beta,19-Epoxypregn-4-ene-3,20-dione

Synonyms:6beta,19-Epoxypregn-4-ene-3,20-dione;(1S,2S,5S,6S,9S,10S,12R)-6-acetyl-5-methyl-19-oxapentacyclo[10.5.2.01,13.02,10.05,9]nonadec-13-en-15-one;CHEBI:79648;Q27148770

Suppliers and Price of 6beta,19-Epoxypregn-4-ene-3,20-dione
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 2 raw suppliers
Chemical Property of 6beta,19-Epoxypregn-4-ene-3,20-dione
Chemical Property:
  • Vapor Pressure:6.98E-10mmHg at 25°C 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:328.20384475
  • Heavy Atom Count:24
  • Complexity:650
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)C1CCC2C1(CCC3C2CC4C5=CC(=O)CCC35CO4)C
  • Isomeric SMILES:CC(=O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@@H]4C5=CC(=O)CC[C@]35CO4)C
Technology Process of 6beta,19-Epoxypregn-4-ene-3,20-dione

There total 9 articles about 6beta,19-Epoxypregn-4-ene-3,20-dione 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 potassium acetate; In methanol; Reflux;
DOI:10.1007/s11172-021-3337-6
Guidance literature:
Multi-step reaction with 6 steps
1: 99 percent / pyridine / 60 h / Ambient temperature
2: 75 percent / N-bromoacetamide, 70percent perchloric acid, water / dioxane / 0.5 h / Ambient temperature
3: 81 percent / lead tetraacetate, iodine / benzene / 1 h / Heating; Irradiation
4: 77 percent / K2CO3, methanol / 2.5 h / Ambient temperature
5: 8 N chromic acid / acetone / 0.33 h / Ambient temperature
6: Li2CO3, LiBr / dimethylformamide / 0.5 h / Heating
With pyridine; lead(IV) acetate; methanol; perchloric acid; water; iodine; chromic acid; lithium carbonate; potassium carbonate; lithium bromide; N-bromoacetamide; In 1,4-dioxane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1007/BF00630435
Guidance literature:
Multi-step reaction with 5 steps
1: 75 percent / N-bromoacetamide, 70percent perchloric acid, water / dioxane / 0.5 h / Ambient temperature
2: 81 percent / lead tetraacetate, iodine / benzene / 1 h / Heating; Irradiation
3: 77 percent / K2CO3, methanol / 2.5 h / Ambient temperature
4: 8 N chromic acid / acetone / 0.33 h / Ambient temperature
5: Li2CO3, LiBr / dimethylformamide / 0.5 h / Heating
With lead(IV) acetate; methanol; perchloric acid; water; iodine; chromic acid; lithium carbonate; potassium carbonate; lithium bromide; N-bromoacetamide; In 1,4-dioxane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1007/BF00630435
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