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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-chlorophenyl)pyridine-3-carboxylic acid

Clc1ccccc1c1cncc(c1)C(=O)O Request for Quotation
Chemical Name: 5-(2-chlorophenyl)pyridine-3-carboxylic acid
CAS Number: 893735-02-9
Product Number: AG00GTFM(AGN-PC-02MG5Z)
Synonyms:
MDL No: MFCD06410264
Molecular Formula: C12H8ClNO2
Molecular Weight: 233.65042

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-Chlorophenyl)nicotinic acid is a versatile compound that finds wide application in chemical synthesis due to its unique chemical properties. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, this compound acts as a valuable precursor in the creation of different heterocyclic structures through various cyclization reactions. Its functional groups enable it to participate in diverse synthetic transformations, offering flexibility in designing and synthesizing novel molecules. Additionally, 5-(2-Chlorophenyl)nicotinic acid is often used as a starting material for the synthesis of ligands, catalysts, and other specialized chemicals, making it a valuable tool for researchers and chemists working in the field of drug discovery, material science, and chemical biology.