Salvigenin

Base Information

Chemical Name:Salvigenin
CAS No.:19103-54-9
Molecular Formula:C18H16 O6
Molecular Weight:328.321
Hs Code.:2914509090
UNII:V522YCM28A
DSSTox Substance ID:DTXSID90172629
Nikkaji Number:J94.489K
Wikidata:Q63398893
Metabolomics Workbench ID:24249
ChEMBL ID:CHEMBL376644
Mol file:19103-54-9.mol

Synonyms:5-hydroxy-6,7,4'-trimethoxy-flavone;5-hydroxy-6,7,4'-trimethoxyflavone;salvigenin

Suppliers and Price of Salvigenin

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

Arctom
Salvigenin ≥98%
10mg
$ 338.00

AvaChem
Salvigenin
1mg
$ 79.00

AvaChem
Salvigenin
5mg
$ 119.00

AvaChem
Salvigenin
10mg
$ 189.00

AvaChem
Salvigenin
20mg
$ 290.00

Biosynth Carbosynth
Salvigenin
1 mg
$ 50.00

Biosynth Carbosynth
Salvigenin
10 mg
$ 250.00

Biosynth Carbosynth
Salvigenin
5 mg
$ 150.00

Biosynth Carbosynth
Salvigenin
2 mg
$ 90.00

Biosynth Carbosynth
Salvigenin
25 mg
$ 500.00

Total 32 raw suppliers

Chemical Property of Salvigenin

Chemical Property:

Vapor Pressure:4.26E-12mmHg at 25°C
Melting Point:188 °C
Boiling Point:535.9°Cat760mmHg
PKA:6.33±0.40(Predicted)
Flash Point:196.9°C
PSA：78.13000
Density:1.314g/cm³
LogP:3.19140
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:328.09468823
Heavy Atom Count:24
Complexity:482

Purity/Quality:

≥98% ^*data from raw suppliers

Salvigenin ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O
Uses Salvigenin is a neuroprotective agent used in the treatment of neurodegenerative diseases acting through oxidative stress on cells.

Technology Process of Salvigenin

There total 15 articles about Salvigenin 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: 99.0%

: 1168-42-9
5,6,7,4'-tetramethoxyflavone

: 19103-54-9
5-hydroxy-4',6,7-trimethoxyflavone

Guidance literature:: With boron tribromide; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1016/j.tet.2004.01.023

Reference yield: 82.0%

: 67-56-1
methanol

: 1390643-64-7
8-bromo-5-hydroxy-7,4'-dimethoxyflavone

: 35095-48-8
6-bromo-5-hydroxy-7,4'-dimethoxyflavone

: 19103-54-9
5-hydroxy-4',6,7-trimethoxyflavone

Guidance literature:: methanol; With sodium methylate; copper(I) bromide; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

8-bromo-5-hydroxy-7,4'-dimethoxyflavone; 6-bromo-5-hydroxy-7,4'-dimethoxyflavone; In N,N-dimethyl-formamide; at 120 ℃; for 5h;
DOI:10.1080/14786419.2011.566224