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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)-

4H-1-Benzopyran-4-one, 7-methoxy-3-phenyl-

COc1ccc2c(c1)occ(c2=O)c1ccccc1 Request for Quotation
Chemical Name: 4H-1-Benzopyran-4-one, 7-methoxy-3-phenyl-
CAS Number: 1621-56-3
Product Number: AG001SR5(AGN-PC-0JU69A)
Synonyms:
MDL No:
Molecular Formula: C16H12O3
Molecular Weight: 252.2647

Identification/Properties

Computed Properties
Molecular Weight:
252.269g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
252.079g/mol
Monoisotopic Mass:
252.079g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
368
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Methoxy-3-phenyl-4H-chromen-4-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and natural product analogs. Its aromatic structure and functional groups make it an ideal precursor for the synthesis of complex molecules with diverse biological activities. In organic chemistry, $name$ is commonly employed as a key intermediate in the preparation of novel heterocyclic compounds through various synthetic routes, such as cyclization reactions and functional group transformations. Additionally, its methoxy and phenyl moieties provide opportunities for further derivatization, allowing for the development of structurally diverse analogs for drug discovery and material science applications. In summary, the strategic utilization of 7-Methoxy-3-phenyl-4H-chromen-4-one in chemical synthesis enables the efficient construction of valuable compounds with potential therapeutic and industrial significance.