Strobochrysin

Base Information

Chemical Name:Strobochrysin
CAS No.:529-52-2
Molecular Formula:C16H12O4
Molecular Weight:268.269
Hs Code.:
ChEMBL ID:CHEMBL163960
DSSTox Substance ID:DTXSID201214666
Metabolomics Workbench ID:23255
Nikkaji Number:J94.472F
Wikidata:Q105340522
Mol file:529-52-2.mol

Synonyms:Strobochrysin;5,7-dihydroxy-6-methyl-2-phenylchromen-4-one;CHEMBL163960;5,7-Dihydroxy-6-methylflavone;529-52-2;5,7-dihydroxy-6-methyl-2-phenyl-4h-chromen-4-one;SCHEMBL6245328;CHEBI:193244;DTXSID201214666;BDBM50423792;LMPK12110170;5,7-Dihydroxy-6-methyl-2-phenyl-4H-1-benzopyran-4-one

Suppliers and Price of Strobochrysin

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 5 raw suppliers

Chemical Property of Strobochrysin

Chemical Property:

PSA：70.67000
LogP:3.17960
XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:268.07355886
Heavy Atom Count:20
Complexity:411

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O

Technology Process of Strobochrysin

There total 15 articles about Strobochrysin 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:

Reference yield: 4.5%

: 480-40-0
5,7-dihydroxy-2-phenyl-chromen-4-one

: 74-88-4
methyl iodide

: 529-52-2
6-Methylchrysine

: 55969-57-8
5-hydroxy-7-methoxy-6-methyl-2-phenyl-chromen-4-one

Guidance literature:: With tetramethyl ammoniumhydroxide; tetraethylammonium iodide; In methanol; for 2h; Heating;
DOI:10.1021/jm991128y

Reference yield:

: 2657-28-5
2,4,6-trihydroxy-3-methyl-acetophenon

: 93-97-0
benzoic acid anhydride

: 529-52-2
6-Methylchrysine

: 55969-56-7
5,7-dihydroxy-8-methyl-2-phenylchromen-4-one

Guidance literature:: With sodium benzoate; at 180 ℃; Erwaermen des Reaktionsprodukts mit aethanol. Kalilauge;

Reference yield:

: 2657-28-5
2,4,6-trihydroxy-3-methyl-acetophenon

: 529-52-2
6-Methylchrysine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine, DMAP / 4 h / Ambient temperature

2: 1.) NaOH, 2.) 96percent aq. H₂SO₄ / 1.) DMSO, 15 min, 2.) AcOH, reflux, 10 min

With pyridine; dmap; sodium hydroxide; sulfuric acid;