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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-(2-methoxyphenyl)pyridine-2-carboxylic acid

COc1ccccc1c1ccc(nc1)C(=O)O Request for Quotation
Chemical Name: 5-(2-methoxyphenyl)pyridine-2-carboxylic acid
CAS Number: 1225539-72-9
Product Number: AG0017FW(AGN-PC-09MPBF)
Synonyms:
MDL No:
Molecular Formula: C13H11NO3
Molecular Weight: 229.2313

Identification/Properties

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


5-(2-Methoxyphenyl)picolinic acid is a versatile compound that finds significant application in chemical synthesis as a key building block. Due to its unique structure and properties, this acid serves as a crucial intermediate in the synthesis of various organic compounds. In particular, it is commonly utilized in the production of pharmaceuticals, agrochemicals, and advanced materials.The presence of a picolinic acid moiety in the molecule imparts specific reactivity and functionality to 5-(2-Methoxyphenyl)picolinic acid, making it a valuable precursor in multi-step organic synthesis processes. Its ability to undergo various chemical transformations such as esterification, amidation, and metal-catalyzed reactions makes it highly versatile for the construction of complex molecular structures.One of the notable applications of 5-(2-Methoxyphenyl)picolinic acid is in the preparation of ligands for coordination chemistry. By modifying the picolinic acid group or the methoxyphenyl substituent, researchers can tailor the properties of the resulting ligands for specific metal binding and catalytic applications. This enables the design and synthesis of custom catalysts with enhanced selectivity and efficiency.Furthermore, the presence of the methoxy group in the aromatic ring of the acid provides additional opportunities for functionalization, allowing for the introduction of various substituents to modulate the compound's physicochemical properties. This flexibility makes 5-(2-Methoxyphenyl)picolinic acid a valuable tool for accessing diverse chemical structures with precise control over stereochemistry and reactivity.Overall, the strategic placement of functional groups in 5-(2-Methoxyphenyl)picolinic acid makes it a key player in the realm of chemical synthesis, offering researchers a powerful platform for creating novel molecules with tailored properties and applications.