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

Base Information
  • Chemical Name:4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-
  • CAS No.:62252-07-7
  • Molecular Formula:C15H12O4
  • Molecular Weight:256.258
  • Hs Code.:
  • ChEMBL ID:CHEMBL4295223
  • DSSTox Substance ID:DTXSID30487825
  • Nikkaji Number:J742.879K
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-

Synonyms:62252-07-7;4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-;7-Hydroxy-2-(2-hydroxyphenyl)chroman-4-one;CHEMBL4295223;7-hydroxy-2-(2-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one;7-hydroxy-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one;DTXSID30487825;BDBM50469098

Suppliers and Price of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-
Chemical Property:
  • 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:343
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3O
Technology Process of 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-hydroxyphenyl)-

There total 11 articles about 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(2-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 potassium hydroxide; In methanol; at 20 ℃; pH=10.0;
DOI:10.1248/cpb.54.1384
Guidance literature:
With hydrogenchloride; sodium acetate; In methanol; for 3h; Reflux;
DOI:10.2174/1570180817999201209204523
Guidance literature:
With sulfuric acid; acetic acid; at 20 ℃; for 36h;
DOI:10.1016/j.ejmech.2018.08.069
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