4-Chloro-2-fluoro-5-methoxybenzaldehyde is an aromatic aldehyde characterized by the presence of a benzene ring substituted with a chloro group, a fluoro group, and a methoxy group, along with an aldehyde functional group. The chloro and fluoro substituents are located at the para and ortho positions relative to the aldehyde group, respectively, while the methoxy group is positioned at the meta location. This compound is typically a pale yellow to light brown solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. It exhibits reactivity typical of aldehydes, including nucleophilic addition and condensation reactions. The presence of electron-withdrawing groups like chlorine and fluorine can influence its reactivity and stability, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, its unique substitution pattern may impart specific biological activities, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound due to its potential toxicity and reactivity.

4-CHLORO-2-FLUORO-5-METHOXY BENZALDEHYDE

177034-24-1: 4-Chloro-2-fluoro-5-methoxybenzaldehyde is an aromatic aldehyde characterized by the presence of a benzene ring substituted with a chloro group, a fluoro group, and a methoxy group, along with an aldehyde functional group. The chloro and fluoro substituents are located at the para and ortho positions relative to the aldehyde group, respectively, while the methoxy group is positioned at the meta location. This compound is typically a pale yellow to light brown solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. It exhibits reactivity typical of aldehydes, including nucleophilic addition and condensation reactions. The presence of electron-withdrawing groups like chlorine and fluorine can influence its reactivity and stability, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, its unique substitution pattern may impart specific biological activities, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound due to its potential toxicity and reactivity.

CAS 177034-24-1

4-CHLORO-2-FLUORO-5-METHOXY BENZALDEHYDE

Benzaldehyde, 4-chloro-2-fluoro-5-methoxy-

Ref: IN-DA00252X

4-Chloro-2-fluoro-5-methoxy benzaldehyde

Ref: 54-PC908646

4-Chloro-2-fluoro-5-methoxy benzaldehyde

Ref: 10-F040423