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CAS 882430-69-5

:

6-acetamido-3-bromo-pyridine-2-carboxylic acid

Description:
6-Acetamido-3-bromo-pyridine-2-carboxylic acid is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at specific positions. The presence of an acetamido group at the 6-position and a bromo group at the 3-position contributes to its unique reactivity and properties. This compound features a carboxylic acid functional group at the 2-position, which enhances its acidity and potential for forming salts or esters. The bromine atom introduces electrophilic characteristics, making it suitable for further chemical modifications. The compound is typically used in pharmaceutical research and development due to its potential biological activity. Its solubility in polar solvents is influenced by the carboxylic acid and acetamido groups, while the bromine substitution can affect its overall stability and reactivity. As with many pyridine derivatives, it may exhibit interesting interactions with biological targets, making it a subject of interest in medicinal chemistry. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.
Formula:C8H7BrN2O3
InChI:InChI=1/C8H7BrN2O3/c1-4(12)10-6-3-2-5(9)7(11-6)8(13)14/h2-3H,1H3,(H,13,14)(H,10,11,12)
SMILES:CC(=Nc1ccc(c(C(=O)O)n1)Br)O
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