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Stypandrol

Base Information Edit
  • Chemical Name:Stypandrol
  • CAS No.:99305-33-6
  • Deprecated CAS:53052-82-7
  • Molecular Formula:C26H22O6
  • Molecular Weight:430.454
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60912756
  • Nikkaji Number:J211.390B
  • Wikidata:Q27108349
  • Metabolomics Workbench ID:68372
  • Mol file:99305-33-6.mol
Stypandrol

Synonyms:Stypandrol;Hemerocallin;99305-33-6;C09971;1-[7-(7-acetyl-1,8-dihydroxy-6-methylnaphthalen-2-yl)-1,8-dihydroxy-3-methylnaphthalen-2-yl]ethanone;AC1L4MYV;SureCN4742401;CHEBI:9294;SCHEMBL4742401;DTXSID60912756;Q27108349;1,1'-(1,1',8,8'-Tetrahydroxy-6,6'-dimethyl[2,2'-binaphthalene]-7,7'-diyl)di(ethan-1-one);1-[7-(7-acetyl-1,8-dihydroxy-6-methyl-2-naphthyl)-1,8-dihydroxy-3-methyl-2-naphthyl]ethanone;Ethanone, 1,1'-(1,1',8,8'-tetrahydroxy-6,6'-dimethyl(2,2'-binaphthalene)-7,7'-diyl)bis-

Suppliers and Price of Stypandrol
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
  • STYPANDROL 95.00%
  • 5MG
  • $ 499.74
Total 1 raw suppliers
Chemical Property of Stypandrol Edit
Chemical Property:
  • PSA:115.06000 
  • LogP:5.50440 
  • XLogP3:5.8
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:430.14163842
  • Heavy Atom Count:32
  • Complexity:663
Purity/Quality:

99% *data from raw suppliers

STYPANDROL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC2=C(C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C(=C4O)C(=O)C)C)O)O)C(=C1C(=O)C)O
Technology Process of Stypandrol

There total 1 articles about Stypandrol 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 boron trichloride; In dichloromethane; for 40h; Ambient temperature;
Guidance literature:
With potassium dihydrogenphosphate; potassiuim nitrosodisulfonate; In acetone; for 2h;
DOI:10.1071/CH9851233
Refernces Edit
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