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4',5,7-Trihydroxyflavan

Base Information
  • Chemical Name:4',5,7-Trihydroxyflavan
  • CAS No.:530-82-5
  • Molecular Formula:C15H14O4
  • Molecular Weight:258.274
  • Hs Code.:
  • ChEMBL ID:CHEMBL471590
  • DSSTox Substance ID:DTXSID80487431
  • Nikkaji Number:J2.325.601K
  • Wikidata:Q82329449
  • Mol file:530-82-5.mol
4',5,7-Trihydroxyflavan

Synonyms:4',5,7-trihydroxyflavan;5,7,4'-trihydroxyflavan;530-82-5;CHEMBL471590;SCHEMBL2595111;DTXSID80487431;MDDPZOZWEZNMTK-UHFFFAOYSA-N

Suppliers and Price of 4',5,7-Trihydroxyflavan
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
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  • price
Total 1 raw suppliers
Chemical Property of 4',5,7-Trihydroxyflavan
Chemical Property:
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:258.08920892
  • Heavy Atom Count:19
  • Complexity:301
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC2=C(C=C(C=C2OC1C3=CC=C(C=C3)O)O)O
Technology Process of 4',5,7-Trihydroxyflavan

There total 7 articles about 4',5,7-Trihydroxyflavan 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 hydrogenchloride; sodium cyanoborohydride; In methanol; for 84h; further solvent;
Guidance literature:
With sodium borohydrid; sulfuric acid; acetic anhydride; sodium hydrogencarbonate; In tetrahydrofuran; ethanol; water; acetic acid;
Guidance literature:
Multi-step reaction with 2 steps
1.1: magnesium bromide dietherate / diethyl ether
1.2: 45 percent / lithium aluminum hydride / diethyl ether / 3 h / -78 - 20 °C
2.1: 75 percent / zinc bromide / CH2Cl2 / 6 h / 20 °C
With magnesium dibromide etherate; zinc dibromide; In diethyl ether; dichloromethane;
DOI:10.1016/j.tet.2006.01.109
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