(2-Chloro-7-methylquinolin-3-yl)methanol is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a chloro substituent at the 2-position and a methyl group at the 7-position of the quinoline ring, along with a hydroxymethyl group (-CH2OH) attached to the nitrogen-containing aromatic system. The presence of the chlorine atom contributes to its reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The hydroxymethyl group can participate in hydrogen bonding, influencing the compound's solubility and interaction with biological targets. This compound may exhibit biological activity, making it of interest for further research in drug development. Its molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and oxidation. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and the presence of other functional groups.

(2-chloro-7-methylquinolin-3-yl)methanol

170848-22-3: (2-Chloro-7-methylquinolin-3-yl)methanol is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a chloro substituent at the 2-position and a methyl group at the 7-position of the quinoline ring, along with a hydroxymethyl group (-CH2OH) attached to the nitrogen-containing aromatic system. The presence of the chlorine atom contributes to its reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The hydroxymethyl group can participate in hydrogen bonding, influencing the compound's solubility and interaction with biological targets. This compound may exhibit biological activity, making it of interest for further research in drug development. Its molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and oxidation. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and the presence of other functional groups.

<p>2-Chloro-7-methylquinoline-3-methanol</p>

CAS 170848-22-3

(2-chloro-7-methylquinolin-3-yl)methanol

2-Chloro-7-methylquinoline-3-methanol

Ref: 54-OR309266