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6-Methylflavonol

Base Information Edit
  • Chemical Name:6-Methylflavonol
  • CAS No.:6971-18-2
  • Molecular Formula:C16H12O3
  • Molecular Weight:252.269
  • Hs Code.:2914400090
  • NSC Number:19029
  • DSSTox Substance ID:DTXSID60280907
  • Nikkaji Number:J435.666G
  • Wikidata:Q63409299
  • Metabolomics Workbench ID:74609
  • ChEMBL ID:CHEMBL483835
  • Mol file:6971-18-2.mol
6-Methylflavonol

Synonyms:6-Methylflavonol;6971-18-2;3-hydroxy-6-methylflavone;3-hydroxy-6-methyl-2-phenyl-4H-chromen-4-one;NSC-19029;NSC19029;CHEMBL483835;Flavone, 3-hydroxy-6-methyl-;SCHEMBL4650064;4H-1-Benzopyran-4-one, 3-hydroxy-6-methyl-2-phenyl-;DTXSID60280907;KLGALCMPMFKGDQ-UHFFFAOYSA-N;TNP00079;NSC 19029;AKOS001679080;CCG-120298;NCGC00017209-01;NCGC00017209-02;NCGC00142419-01;Q63409299;4H-1-Benzopyran-4-one (9CI), 3-hydroxy-6-methyl-2-phenyl-

Suppliers and Price of 6-Methylflavonol
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 3 raw suppliers
Chemical Property of 6-Methylflavonol Edit
Chemical Property:
  • Vapor Pressure:7.59E-08mmHg at 25°C 
  • Boiling Point:421.2°C at 760 mmHg 
  • Flash Point:159.8°C 
  • PSA:50.44000 
  • Density:1.324g/cm3 
  • LogP:3.47400 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:252.078644241
  • Heavy Atom Count:19
  • Complexity:393
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=CC2=C(C=C1)OC(=C(C2=O)O)C3=CC=CC=C3
Technology Process of 6-Methylflavonol

There total 8 articles about 6-Methylflavonol 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 Trimethyl borate; dihydrogen peroxide; acetic acid; lithium diisopropyl amide; Multistep reaction; 1.) THF/hexane, -78 deg C, 35 min; 2.) THF, -78 deg C;
Guidance literature:
Multi-step reaction with 4 steps
1.1: pyridine
2.1: KOH / pyridine
3.1: AcOH; H2SO4
4.1: PhI(OAc)2; KOH / methanol
4.2: HCl / acetone
With pyridine; potassium hydroxide; [bis(acetoxy)iodo]benzene; sulfuric acid; acetic acid; In pyridine; methanol; 1.1: Esterification / 2.1: Cyclization / 3.1: Dehydration / 4.1: Oxidation / 4.2: Hydrolysis;
DOI:10.1016/S0968-0896(99)00261-8
Guidance literature:
Multi-step reaction with 3 steps
1.1: KOH / pyridine
2.1: AcOH; H2SO4
3.1: PhI(OAc)2; KOH / methanol
3.2: HCl / acetone
With potassium hydroxide; [bis(acetoxy)iodo]benzene; sulfuric acid; acetic acid; In pyridine; methanol; 1.1: Cyclization / 2.1: Dehydration / 3.1: Oxidation / 3.2: Hydrolysis;
DOI:10.1016/S0968-0896(99)00261-8
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