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4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-

Base Information Edit
  • Chemical Name:4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-
  • CAS No.:41680-09-5
  • Molecular Formula:C15H12O4
  • Molecular Weight:256.258
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90274339,DTXSID90961898
  • Nikkaji Number:J461.942K
  • Wikidata:Q72487544
  • Pharos Ligand ID:TJSMXHLNWJFQ
  • Metabolomics Workbench ID:129965
  • ChEMBL ID:CHEMBL271939
  • Mol file:41680-09-5.mol
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-

Synonyms:7,4'-dihydroxyflavanone;liquiritigenin

Suppliers and Price of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-
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
Total 8 raw suppliers
Chemical Property of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- Edit
Chemical Property:
  • PSA:66.76000 
  • LogP:2.80430 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:256.07355886
  • Heavy Atom Count:19
  • Complexity:335
Purity/Quality:

more than 97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O
Technology Process of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-

There total 59 articles about 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 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; In ethanol; water; for 1h; Reflux;
DOI:10.1016/j.ejmech.2010.04.036
Guidance literature:
With hydrogenchloride; In methanol; water; for 48h; Reflux;
DOI:10.1039/c4ra10842f
Guidance literature:
With methanol; sodium tetrahydroborate; In dichloromethane; at -30 ℃; for 2h; Reagent/catalyst; Temperature;
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