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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-Pyridinecarboxylic acid, 2-(4-fluorophenyl)-

Fc1ccc(cc1)c1ncccc1C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 2-(4-fluorophenyl)-
CAS Number: 101419-78-7
Product Number: AG0004FT(AGN-PC-00N8P9)
Synonyms:
MDL No:
Molecular Formula: C12H8FNO2
Molecular Weight: 217.1958

Identification/Properties

Computed Properties
Molecular Weight:
217.199g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
217.054g/mol
Monoisotopic Mass:
217.054g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
251
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


2-(4-Fluorophenyl)nicotinic acid plays a crucial role in chemical synthesis as a versatile building block in the creation of various organic compounds. Its unique structure, incorporating both a fluorine-substituted phenyl ring and a nicotinic acid moiety, enables it to participate in a wide range of reactions to form complex molecules. This compound is commonly employed in the pharmaceutical industry for the synthesis of drug candidates and intermediates. Additionally, it is utilized in academic research settings to explore new synthetic methodologies and develop innovative chemical processes. The presence of the fluorine atom enhances the compound's reactivity and selectivity in reactions, making it a valuable tool for organic chemists seeking to design and construct novel molecules with potential applications in medicine, materials science, and beyond.