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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)-

5-fluoro-6-methoxypyridine-3-carboxylic acid

COc1ncc(cc1F)C(=O)O Request for Quotation
Chemical Name: 5-fluoro-6-methoxypyridine-3-carboxylic acid
CAS Number: 953780-42-2
Product Number: AG00IJ0G(AGN-PC-0ALRWI)
Synonyms:
MDL No:
Molecular Formula: C7H6FNO3
Molecular Weight: 171.1258

Identification/Properties

Computed Properties
Molecular Weight:
171.127g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
171.033g/mol
Monoisotopic Mass:
171.033g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-6-methoxynicotinic acid is a versatile building block in chemical synthesis due to its unique structure and reactivity. As a fluorinated derivative of nicotinic acid, this compound offers several applications in organic chemistry.One of the key uses of 5-Fluoro-6-methoxynicotinic acid is as a precursor in the synthesis of various pharmaceutical compounds. Its fluorine substituent can serve as a strategic handle for further functionalization, allowing for the introduction of diverse chemical groups to modulate the properties of the final products. Additionally, the methoxy group provides an opportunity for additional modifications, expanding the scope of potential molecules that can be derived from this starting material.Furthermore, the presence of the nicotinic acid scaffold in 5-Fluoro-6-methoxynicotinic acid offers potential biological activity, making it a valuable intermediate in the design and development of bioactive molecules. By leveraging the structural features of this compound, researchers can access new chemical entities with tailored properties for applications in medicinal chemistry and drug discovery.Overall, the application of 5-Fluoro-6-methoxynicotinic acid in chemical synthesis highlights its significance in the creation of complex molecules with potential pharmacological relevance, showcasing its role as a valuable tool for synthetic chemists and pharmaceutical researchers.