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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)-

1-(4-fluorophenyl)-2-oxopyridine-4-carbonitrile

N#Cc1ccn(c(=O)c1)c1ccc(cc1)F Request for Quotation
Chemical Name: 1-(4-fluorophenyl)-2-oxopyridine-4-carbonitrile
CAS Number: 929000-78-2
Product Number: AG003CZH(AGN-PC-058CNP)
Synonyms:
MDL No:
Molecular Formula: C12H7FN2O
Molecular Weight: 214.1952

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
214.199g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
214.054g/mol
Monoisotopic Mass:
214.054g/mol
Topological Polar Surface Area:
44.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
397
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#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Fluorophenyl)-2-oxo-1,2-dihydropyridine-4-carbonitrile, commonly referred to as $name$, is a versatile compound that finds extensive application in chemical synthesis processes. This compound serves as a crucial building block for the synthesis of various complex organic molecules, owing to its unique structural properties and reactivity.In organic synthesis, $name$ is frequently utilized as a key intermediate in the preparation of biologically active compounds, pharmaceuticals, and agrochemicals. Its strategic placement of functional groups allows for the introduction of diverse substituents, facilitating the generation of structurally diverse molecules with potential therapeutic properties.Moreover, the presence of the fluoro-substituted phenyl ring confers specific reactivity patterns to $name$, making it a valuable precursor in the development of new materials and fine chemicals. The carbonitrile moiety in the molecule further enhances its utility by providing sites for further functionalization through a variety of chemical transformations.Overall, the strategic incorporation of 1-(4-Fluorophenyl)-2-oxo-1,2-dihydropyridine-4-carbonitrile into synthetic pathways enables chemists to access a wide array of novel compounds with tailored properties, thereby driving innovation in the field of chemical synthesis.