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CAS 871269-03-3

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2-(acetylamino)-5-bromopyridine-4-carboxylic acid

Description:
2-(Acetylamino)-5-bromopyridine-4-carboxylic acid is a chemical compound characterized by its pyridine ring structure, which is substituted at specific positions with an acetylamino group, a bromine atom, and a carboxylic acid group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential solubility in polar solvents due to the presence of the carboxylic acid functional group. The acetylamino group contributes to its reactivity and may influence its biological activity, making it of interest in pharmaceutical research. The bromine atom introduces a halogen, which can enhance the compound's reactivity in various chemical reactions, such as nucleophilic substitutions. Additionally, the presence of multiple functional groups suggests that this compound may participate in hydrogen bonding, affecting its physical properties like melting point and solubility. Overall, 2-(acetylamino)-5-bromopyridine-4-carboxylic acid is a versatile compound with potential applications in medicinal chemistry and organic synthesis.
Formula:C8H7BrN2O3
InChI:InChI=1/C8H7BrN2O3/c1-4(12)11-7-2-5(8(13)14)6(9)3-10-7/h2-3H,1H3,(H,13,14)(H,10,11,12)
SMILES:CC(=Nc1cc(c(cn1)Br)C(=O)O)O
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