5-Chloro-6-(2-methylpropoxy)pyridine-3-carboxylic acid is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a carboxylic acid functional group (-COOH) at the 3-position of the pyridine ring contributes to its acidic properties, making it capable of donating protons in solution. The 5-chloro substituent introduces a chlorine atom, which can influence the compound's reactivity and polarity. Additionally, the 6-position features a 2-methylpropoxy group, which is an alkoxy substituent that can enhance the compound's lipophilicity and potentially affect its solubility in organic solvents. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical research. Its molecular interactions, stability, and reactivity can be influenced by the presence of the chlorine atom and the alkoxy group, which may also affect its pharmacokinetic properties. Overall, this compound's unique structure positions it as a candidate for various applications in medicinal chemistry and agrochemicals.

5-chloro-6-(2-methylpropoxy)pyridine-3-carboxylic acid

1008769-66-1: 5-Chloro-6-(2-methylpropoxy)pyridine-3-carboxylic acid is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a carboxylic acid functional group (-COOH) at the 3-position of the pyridine ring contributes to its acidic properties, making it capable of donating protons in solution. The 5-chloro substituent introduces a chlorine atom, which can influence the compound's reactivity and polarity. Additionally, the 6-position features a 2-methylpropoxy group, which is an alkoxy substituent that can enhance the compound's lipophilicity and potentially affect its solubility in organic solvents. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical research. Its molecular interactions, stability, and reactivity can be influenced by the presence of the chlorine atom and the alkoxy group, which may also affect its pharmacokinetic properties. Overall, this compound's unique structure positions it as a candidate for various applications in medicinal chemistry and agrochemicals.

CAS 1008769-66-1

5-chloro-6-(2-methylpropoxy)pyridine-3-carboxylic acid

5-Chloro-6-(2-methylpropoxy)pyridine-3-carboxylic acid

Ref: 3D-IQB76966