Isokaempferide

Base Information

Chemical Name:Isokaempferide
CAS No.:1592-70-7
Molecular Formula:C16H12O6
Molecular Weight:300.268
Hs Code.:2914509090
European Community (EC) Number:803-276-8
ChEMBL ID:CHEMBL165064
DSSTox Substance ID:DTXSID90166609
Metabolomics Workbench ID:25771
Nikkaji Number:J94.493I
Wikidata:Q27105473
Mol file:1592-70-7.mol

Synonyms:5,7,4'-trihydroxy-3-methoxyflavone;isokaempferide

Suppliers and Price of Isokaempferide

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

Sigma-Aldrich
Isokaempferide ≥90% (LC/MS-ELSD)
1mg
$ 370.00

Crysdot
Isokaempferide 95+%
5mg
$ 730.00

Arctom
Isokaempferide
5mg
$ 368.00

Total 24 raw suppliers

Chemical Property of Isokaempferide

Chemical Property:

Melting Point:>300℃
Boiling Point:586.2 °C at 760 mmHg
PKA:6.34±0.40(Predicted)
Flash Point:224.1 °C
PSA：100.13000
Density:1.58 g/cm³
LogP:2.58540
Storage Temp.:?20°C
XLogP3:2.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:300.06338810
Heavy Atom Count:22
Complexity:465

Purity/Quality:

99% ^*data from raw suppliers

Isokaempferide ≥90% (LC/MS-ELSD) ^*data from reagent suppliers

Safty Information:

Pictogram(s): T,N
Hazard Codes:T,N
Statements: 25-50
Safety Statements: 45-61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O
Uses Isokaempferide is a bioactive flavonoid with antioxidant and anticholinesterase activity.

Technology Process of Isokaempferide

There total 15 articles about Isokaempferide 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: 91.0%

: 3-O-methyl-7-O-benzylkaempferol

: 1592-70-7
3-methoxy-5,7,4'-trihydroxyflavone

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate; at 20 ℃; for 5h;
DOI:10.3762/bjoc.11.33

Reference yield: 45.0%

: 1486-59-5
4'-(benzyloxy)-5,7-dihydroxy-3-methoxyflavone

: 1592-70-7
3-methoxy-5,7,4'-trihydroxyflavone

Guidance literature:: With hydrogenchloride; acetic acid; for 3h; Heating;
DOI:10.1021/jm00106a039

Reference yield:

: 520-18-3
kaempferol

: 1592-70-7
3-methoxy-5,7,4'-trihydroxyflavone

: 491-54-3
4'-O-methylkaempferol

Guidance literature:: With O-methyl transferase from cell-free extract of Citrus mitis; <(14)CH3>-S-adenosyl-L-methionine; 2-hydroxyethanethiol; In water; dimethyl sulfoxide; at 35 ℃; for 0.5h; Product distribution; pH 7.5 buffer;
DOI:10.1016/0031-9422(80)85102-8