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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3,5-dihydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one

COc1ccc(cc1)c1oc2cc(OC)cc(c2c(=O)c1O)O Request for Quotation
Chemical Name: 3,5-dihydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one
CAS Number: 15486-33-6
Product Number: AG00APXL(AGN-PC-0LQGZN)
Synonyms:
MDL No:
Molecular Formula: C17H14O6
Molecular Weight: 314.2895

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dihydroxy-4',7-Dimethoxyflavone is a versatile compound commonly used in chemical synthesis as a key building block in the development of novel pharmaceuticals and agrochemicals. This compound serves as a crucial intermediate in the production of various bioactive molecules due to its unique molecular structure and reactivity. In particular, 3,5-Dihydroxy-4',7-Dimethoxyflavone can be employed in the synthesis of natural product analogs, medicinal compounds, and plant protection agents through diverse chemical transformations such as acylation, alkylation, and oxidative coupling reactions. Its functional groups and aromatic system make it a valuable substrate for derivatization, enabling chemists to modify its properties for specific applications. With its significance in the field of chemical synthesis, 3,5-Dihydroxy-4',7-Dimethoxyflavone plays a pivotal role in expanding the scope of organic chemistry research and innovation.