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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-chloro-2-methylpyridine-4-carboxylic acid

Cc1ncc(c(c1)C(=O)O)Cl Request for Quotation
Chemical Name: 5-chloro-2-methylpyridine-4-carboxylic acid
CAS Number: 1060810-03-8
Product Number: AG008UB3(AGN-PC-0BS74C)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO2
Molecular Weight: 171.5810

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Chemical Structure


5-Chloro-2-methylisonicotinic acid is a versatile chemical compound commonly used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials. The presence of the chloro and methyl substituents on the isonicotinic acid backbone enhances its compatibility for diverse chemical reactions, allowing for the efficient formation of complex molecular structures. Additionally, the chloro group provides a handle for further derivatization, enabling the introduction of different functional groups for specific applications. Whether employed as a key intermediate in the pharmaceutical industry or utilized in academic research settings, 5-Chloro-2-methylisonicotinic acid continues to play a crucial role in advancing chemical synthesis methodologies and expanding the frontiers of organic chemistry.