Agecorynin C

Base Information

Chemical Name:Agecorynin C
CAS No.:70460-31-0
Molecular Formula:C22H24O9
Molecular Weight:432.427
Hs Code.:
NSC Number:83279
UNII:Q44S2K78D4
DSSTox Substance ID:DTXSID10220732
Nikkaji Number:J2.790.750D
Wikidata:Q27148537
Metabolomics Workbench ID:24586
ChEMBL ID:CHEMBL521296

Synonyms:Agecorynin C;70460-31-0;5,6,7,8-Tetramethoxy-2-(2,4,5-trimethoxyphenyl)-4H-chromen-4-one;Q44S2K78D4;NSC 83279;NSC-83279;UNII-Q44S2K78D4;CHEBI:79466;5,6,7,8-tetramethoxy-2-(2,4,5-trimethoxyphenyl)chromen-4-one;2-(2,4,5-Trimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one;NSC83279;5,6,7,8-Tetramethoxy-2-(2,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one;CHEMBL521296;DTXSID10220732;LMPK12111503;NCI60_041832;2',4',5,5',6,7,8-heptamethoxyflavone;Q27148537;4H-1-Benzopyran-4-one,6,7,8-tetramethoxy-2-(2,4,5-trimethoxyphenyl)-;4H-1-Benzopyran-4-one, 5,6,7,8-tetramethoxy-2-(2,4,5-trimethoxyphenyl)-

Suppliers and Price of Agecorynin C

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 Agecorynin C

Chemical Property:

Vapor Pressure:2.9E-15mmHg at 25°C
Boiling Point:619.3°Cat760mmHg
Flash Point:268.3°C
Density:1.245g/cm³
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:8
Exact Mass:432.14203234
Heavy Atom Count:31
Complexity:639

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC

Technology Process of Agecorynin C

There total 7 articles about Agecorynin C 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: 80.0%

: 77084-18-5
2-hydroxy-3,4,5,6-tetramethoxy-2',4',5'-trimethoxydibenzoylmethane

: 70460-31-0
2',4',5,5',6,7,8-heptamethoxyflavone

Guidance literature:: With sodium acetate; acetic acid; for 4h; Heating;

Reference yield:

: 3162-28-5
2-hydroxy-3,4,5,6-tetramethoxyacetophenone

: 70460-31-0
2',4',5,5',6,7,8-heptamethoxyflavone

Guidance literature:: Multi-step reaction with 2 steps

1: 0.16 g

2: 20 mg / DDQ

With 2,3-dicyano-5,6-dichloro-p-benzoquinone;
DOI:10.1248/cpb.32.4935

Reference yield:

: 7507-98-4
1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone

: 70460-31-0
2',4',5,5',6,7,8-heptamethoxyflavone

Guidance literature:: Multi-step reaction with 5 steps

1: 33.3 percent / potassium persulphate, sodium hydroxide / H₂O

2: 80 percent / methanol; diethyl ether

3: 85 percent / pyridine / 1 h / 100 °C

4: 75 percent / potassium hydroxide / pyridine / 4 h / 60 °C

5: 80 percent / glacial acetic acid, sodium acetate / 4 h / Heating

With pyridine; potassium hydroxide; sodium hydroxide; potassium peroxomonosulphate; sodium acetate; acetic acid; In pyridine; methanol; diethyl ether; water;