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Gitoxigenin

Base Information Edit
  • Chemical Name:Gitoxigenin
  • CAS No.:545-26-6
  • Molecular Formula:C23H34 O5
  • Molecular Weight:390.52
  • Hs Code.:
  • European Community (EC) Number:208-886-2
  • NSC Number:407807
  • UNII:G36K2H8SME
  • DSSTox Substance ID:DTXSID20878642
  • Nikkaji Number:J6.421A
  • Wikidata:Q1527718
  • Metabolomics Workbench ID:35217
  • ChEMBL ID:CHEMBL464658
  • Mol file:545-26-6.mol
Gitoxigenin

Synonyms:gitoxigenin

Suppliers and Price of Gitoxigenin
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
  • TRC
  • Gitoxigenin
  • 5mg
  • $ 1890.00
  • American Custom Chemicals Corporation
  • GITOXIGENIN 95.00%
  • 10MG
  • $ 582.97
Total 10 raw suppliers
Chemical Property of Gitoxigenin Edit
Chemical Property:
  • Vapor Pressure:1.97E-16mmHg at 25°C 
  • Melting Point:~230 °C
     
  • Refractive Index:1.6120 (estimate) 
  • Boiling Point:591°Cat760mmHg 
  • PKA:14.56±0.70(Predicted) 
  • Flash Point:203.6°C 
  • PSA:86.99000 
  • Density:1.297g/cm3 
  • LogP:2.57510 
  • Storage Temp.:−20°C 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:390.24062418
  • Heavy Atom Count:28
  • Complexity:718
Purity/Quality:

98%,99%, *data from raw suppliers

Gitoxigenin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 23/24/25 
  • Safety Statements: 36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=CC(=O)OC5)O)O)C)O
  • Isomeric SMILES:C[C@]12CC[C@@H](C[C@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@@]3(C[C@@H]([C@@H]4C5=CC(=O)OC5)O)O)C)O
  • Uses Gitoxigenin is a related compound of Digitoxigenin, which has been used in a study to assess its stereochemical effects in cancer cytotoxicity. Digitoxigenin has also been used in a study to investigate the advantage of gold(I)-catalyzed glycosidation of glycosyl o-alkyl benzoates to assemble digitoxin.
Technology Process of Gitoxigenin

There total 7 articles about Gitoxigenin 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: 68.0%

Guidance literature:
With sulfuric acid; In methanol; for 2.5h; Heating;
DOI:10.1021/jm00156a017
Guidance literature:
With trifluoroacetic acid; In butan-1-ol; at 200 ℃; for 1.5h;
DOI:10.3390/molecules26103030
Guidance literature:
for 432h; Further byproducts given; Strophantus divaricatus cultures, 5percent Twen 80;
DOI:10.1016/0031-9422(91)84197-Z
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