2,6-Dichloro-4-(dimethylamino)nicotinaldehyde is a chemical compound that belongs to the class of nicotinic derivatives. It features a pyridine ring with two chlorine substituents at the 2 and 6 positions, and a dimethylamino group at the 4 position, along with an aldehyde functional group. This compound is typically characterized by its potential biological activity, particularly in the context of medicinal chemistry, where it may exhibit properties relevant to drug development. The presence of the dimethylamino group can enhance its lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, the dichloro substituents may impart unique reactivity and stability characteristics. As with many organic compounds, its solubility, melting point, and reactivity can vary based on environmental conditions and the presence of other substances. Safety data should be consulted for handling and usage, as halogenated compounds can pose specific health and environmental risks. Overall, 2,6-dichloro-4-(dimethylamino)nicotinaldehyde is of interest in various chemical and pharmaceutical applications.

2,6-dichloro-4-(dimethylamino)nicotinaldehyde

1823371-33-0: 2,6-Dichloro-4-(dimethylamino)nicotinaldehyde is a chemical compound that belongs to the class of nicotinic derivatives. It features a pyridine ring with two chlorine substituents at the 2 and 6 positions, and a dimethylamino group at the 4 position, along with an aldehyde functional group. This compound is typically characterized by its potential biological activity, particularly in the context of medicinal chemistry, where it may exhibit properties relevant to drug development. The presence of the dimethylamino group can enhance its lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, the dichloro substituents may impart unique reactivity and stability characteristics. As with many organic compounds, its solubility, melting point, and reactivity can vary based on environmental conditions and the presence of other substances. Safety data should be consulted for handling and usage, as halogenated compounds can pose specific health and environmental risks. Overall, 2,6-dichloro-4-(dimethylamino)nicotinaldehyde is of interest in various chemical and pharmaceutical applications.

CAS 1823371-33-0

2,6-dichloro-4-(dimethylamino)nicotinaldehyde

2,6-Dichloro-4-(dimethylamino)nicotinaldehyde

Ref: IN-DA01DTRW

2,6-Dichloro-4-(dimethylamino)nicotinaldehyde

Ref: 54-OR510157

2,6-Dichloro-4-(dimethylamino)nicotinaldehyde

Ref: 10-F601343