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17-Deoxyestradiol

Base Information Edit
  • Chemical Name:17-Deoxyestradiol
  • CAS No.:53-63-4
  • Molecular Formula:C18H24O
  • Molecular Weight:256.388
  • Hs Code.:
  • NSC Number:57428
  • UNII:73A01W88SP
  • DSSTox Substance ID:DTXSID1022471
  • Nikkaji Number:J71.376G
  • Wikidata:Q27132230
  • Pharos Ligand ID:728Z6GZBFC3B
  • Metabolomics Workbench ID:62453
  • ChEMBL ID:CHEMBL261406
  • Mol file:53-63-4.mol
17-Deoxyestradiol

Synonyms:17-deoxyestradiol;17-desoxyestradiol

Suppliers and Price of 17-Deoxyestradiol
Supply Marketing:Edit
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
  • 1,3,5(10)-ESTRATRIEN-3-OL 95.00%
  • 5MG
  • $ 450.21
Total 4 raw suppliers
Chemical Property of 17-Deoxyestradiol Edit
Chemical Property:
  • Vapor Pressure:5.76E-07mmHg at 25°C 
  • Melting Point:135.5-137 °C 
  • Boiling Point:399.8°Cat760mmHg 
  • PKA:10.30±0.40(Predicted) 
  • Flash Point:188.8°C 
  • PSA:20.23000 
  • Density:1.087g/cm3 
  • LogP:4.63840 
  • XLogP3:5.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:256.182715385
  • Heavy Atom Count:19
  • Complexity:352
Purity/Quality:

98%min *data from raw suppliers

1,3,5(10)-ESTRATRIEN-3-OL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCCC1C3CCC4=C(C3CC2)C=CC(=C4)O
  • Isomeric SMILES:C[C@@]12CCC[C@H]1[C@@H]3CCC4=C([C@H]3CC2)C=CC(=C4)O
Technology Process of 17-Deoxyestradiol

There total 21 articles about 17-Deoxyestradiol 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 palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 3h; under 15001.5 Torr;
DOI:10.1016/j.steroids.2016.05.010

Reference yield: 93.0%

Guidance literature:
With bismuth(III) oxide; N-ethyl-N,N-diisopropylamine; para-thiocresol; In dichloromethane; for 2h; Irradiation;

Reference yield: 91.0%

Guidance literature:
Estrone; With hydrazine hydrate; potassium hydroxide; In butan-1-ol; diethylene glycol; for 0.5h; Reflux;
In water; butan-1-ol; at 200 ℃; for 2h;
DOI:10.1021/acs.joc.9b00786
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