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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-Pyridinecarboxylicacid, 4-fluoro-

OC(=O)c1cnccc1F Request for Quotation
Chemical Name: 3-Pyridinecarboxylicacid, 4-fluoro-
CAS Number: 152126-33-5
Product Number: AG007JRT(AGN-PC-0KKP6J)
Synonyms:
MDL No:
Molecular Formula: C6H4FNO2
Molecular Weight: 141.0999

Identification/Properties

Computed Properties
Molecular Weight:
141.101g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
141.023g/mol
Monoisotopic Mass:
141.023g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
140
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoronicotinic acid is a versatile chemical compound widely utilized in chemical synthesis processes. Due to its unique properties, it serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its presence as a fluorinated derivative of nicotinic acid imparts specific reactivity and functionality that is advantageous in organic synthesis. The introduction of a fluorine atom enhances the molecule's stability and alters its electronic properties, thereby influencing its behavior in reactions. In chemical synthesis, 4-Fluoronicotinic acid acts as a valuable intermediate for the preparation of complex organic molecules with advanced functionalities. It can undergo diverse chemical transformations such as nucleophilic substitution, metal-catalyzed coupling reactions, and various derivatization processes. The presence of the fluorine substituent offers a handle for selective modifications and enables the incorporation of fluorine-containing motifs into target molecules. This versatility makes 4-Fluoronicotinic acid a sought-after reagent in medicinal chemistry, material science, and other research fields where precise control over molecular structure is essential.Furthermore, the unique properties of 4-Fluoronicotinic acid make it a valuable tool for the synthesis of novel fluorinated compounds with potential biological activities or specific physicochemical properties. Its ability to serve as a precursor for diverse functional groups and structural motifs expands the possibilities for designing and developing new molecules with desired characteristics. By leveraging the synthetic potential of 4-Fluoronicotinic acid, researchers can access a wide range of chemical space and explore innovative pathways towards the discovery of novel compounds for various applications.