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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-(4-hydroxyphenyl)pyridine-3-carboxylic acid

Oc1ccc(cc1)c1cncc(c1)C(=O)O Request for Quotation
Chemical Name: 5-(4-hydroxyphenyl)pyridine-3-carboxylic acid
CAS Number: 1181566-40-4
Product Number: AG0076XI(AGN-PC-0NT0YU)
Synonyms:
MDL No:
Molecular Formula: C12H9NO3
Molecular Weight: 215.2048

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-(4-Hydroxyphenyl)nicotinic acid is a versatile compound used in chemical synthesis for various applications. With its unique structure combining a nicotinic acid backbone with a hydroxyphenyl group, this compound plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 5-(4-Hydroxyphenyl)nicotinic acid serves as a valuable building block for constructing complex molecules. Its hydroxyphenyl group can participate in a range of reactions such as Heck coupling, Suzuki-Miyaura cross-coupling, and nucleophilic substitution, allowing for the introduction of functionalities at specific positions within a molecule.Furthermore, the presence of nicotinic acid in the compound offers additional reactivity, enabling the formation of heterocyclic structures important in drug design and synthesis. This dual functionality makes 5-(4-Hydroxyphenyl)nicotinic acid an attractive starting material for the preparation of pharmacologically active compounds and new chemical entities.Overall, the application of 5-(4-Hydroxyphenyl)nicotinic acid in chemical synthesis provides chemists with a powerful tool to access diverse molecular architectures and develop innovative molecules with potential therapeutic or industrial significance.