4-Chloro-5-fluoro-2-hydroxybenzaldehyde is an organic compound characterized by the presence of a benzaldehyde functional group, which includes a carbonyl (aldehyde) group attached to a benzene ring. The compound features a hydroxyl (-OH) group and two halogen substituents: a chlorine atom and a fluorine atom, which are located at the 4 and 5 positions of the benzene ring, respectively. This substitution pattern can influence the compound's reactivity, polarity, and solubility. The hydroxyl group contributes to its potential as a hydrogen bond donor, while the halogens can affect electronic properties and steric hindrance. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the presence of both halogens and a hydroxyl group may enhance its reactivity in synthetic applications. Overall, 4-chloro-5-fluoro-2-hydroxybenzaldehyde is a versatile compound with potential applications in organic synthesis and medicinal chemistry.

4-chloro-5-fluoro-2-hydroxybenzladehyde

1205551-36-5: 4-Chloro-5-fluoro-2-hydroxybenzaldehyde is an organic compound characterized by the presence of a benzaldehyde functional group, which includes a carbonyl (aldehyde) group attached to a benzene ring. The compound features a hydroxyl (-OH) group and two halogen substituents: a chlorine atom and a fluorine atom, which are located at the 4 and 5 positions of the benzene ring, respectively. This substitution pattern can influence the compound's reactivity, polarity, and solubility. The hydroxyl group contributes to its potential as a hydrogen bond donor, while the halogens can affect electronic properties and steric hindrance. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the presence of both halogens and a hydroxyl group may enhance its reactivity in synthetic applications. Overall, 4-chloro-5-fluoro-2-hydroxybenzaldehyde is a versatile compound with potential applications in organic synthesis and medicinal chemistry.

CAS 1205551-36-5

4-chloro-5-fluoro-2-hydroxybenzladehyde

4-Chloro-5-fluoro-2-hydroxy-benzaldehyde

Ref: IN-DA0092IS

4-Chloro-5-fluoro-2-hydroxybenzaldehyde

Ref: 54-PC909159

4-Chloro-5-fluoro-2-hydroxybenzaldehyde

Ref: 10-F458109