2-Chloro-6-fluoronicotinaldehyde is an organic compound characterized by its pyridine ring structure, which features both a chlorine and a fluorine substituent, as well as an aldehyde functional group. The presence of the chlorine atom at the 2-position and the fluorine atom at the 6-position of the pyridine ring contributes to its unique reactivity and potential applications in various chemical reactions. This compound is typically a pale yellow to light brown solid, and it is soluble in organic solvents such as ethanol and dichloromethane. Its aldehyde group makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The compound's properties, including its melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. As with many halogenated compounds, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and safety precautions are essential due to the potential toxicity associated with halogenated organic compounds.

2-chloro-6-fluoronicotinaldehyde

1227563-22-5: 2-Chloro-6-fluoronicotinaldehyde is an organic compound characterized by its pyridine ring structure, which features both a chlorine and a fluorine substituent, as well as an aldehyde functional group. The presence of the chlorine atom at the 2-position and the fluorine atom at the 6-position of the pyridine ring contributes to its unique reactivity and potential applications in various chemical reactions. This compound is typically a pale yellow to light brown solid, and it is soluble in organic solvents such as ethanol and dichloromethane. Its aldehyde group makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The compound's properties, including its melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. As with many halogenated compounds, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and safety precautions are essential due to the potential toxicity associated with halogenated organic compounds.

3-Pyridinecarboxaldehyde, 2-chloro-6-fluoro-

2-Chloro-6-fluoro-3-pyridinecarboxaldehyde

CAS 1227563-22-5

2-chloro-6-fluoronicotinaldehyde

3-Pyridinecarboxaldehyde, 2-chloro-6-fluoro-

Ref: IN-DA000JAJ

2-Chloro-6-fluoro-3-pyridinecarboxaldehyde

Ref: 54-PC101326

2-CHLORO-6-FLUORONICOTINALDEHYDE

Ref: 10-F500504