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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, 6-fluoro-4-methyl-

Cc1cc(F)ncc1C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylicacid, 6-fluoro-4-methyl-
CAS Number: 944582-95-0
Product Number: AG00II6P(AGN-PC-07XU7Y)
Synonyms:
MDL No:
Molecular Formula: C7H6FNO2
Molecular Weight: 155.1264

Identification/Properties

Computed Properties
Molecular Weight:
155.128g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
155.038g/mol
Monoisotopic Mass:
155.038g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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


6-Fluoro-4-methylnicotinic acid, also known as $name$, is a versatile intermediate in chemical synthesis. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and functional materials. With its unique structural properties, $name$ is widely utilized as a building block in organic reactions to introduce fluorine and methyl groups into target molecules. In chemical synthesis, $name$ serves as a key starting material for the preparation of novel compounds with enhanced biological or physical properties. Its strategic placement of the fluorine and methyl substituents allows for the modulation of the compound's reactivity, lipophilicity, and overall pharmacokinetic profile. Moreover, the presence of a fluoro-substituted aromatic ring in $name$ imparts valuable properties such as increased metabolic stability and improved binding affinity in drug design. By incorporating 6-Fluoro-4-methylnicotinic acid into the molecular structure of organic compounds, chemists can fine-tune the properties of the final products to meet specific requirements for various applications in the fields of medicine, agriculture, and materials science.