5-(4-Chlorophenyl)isoxazole-3-carbaldehyde is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a 4-chlorophenyl group indicates that a chlorinated phenyl substituent is attached to the isoxazole at the 5-position, contributing to its aromatic properties and potentially influencing its reactivity and biological activity. The aldehyde functional group at the 3-position of the isoxazole ring is significant for its reactivity, allowing for various chemical transformations, such as condensation reactions. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in the development of agrochemicals or pharmaceuticals. Additionally, the presence of the chlorine atom can enhance lipophilicity and influence the compound's interaction with biological targets. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.

5-(4-chlorophenyl)isoxazole-3-carbaldehyde

763109-09-7: 5-(4-Chlorophenyl)isoxazole-3-carbaldehyde is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a 4-chlorophenyl group indicates that a chlorinated phenyl substituent is attached to the isoxazole at the 5-position, contributing to its aromatic properties and potentially influencing its reactivity and biological activity. The aldehyde functional group at the 3-position of the isoxazole ring is significant for its reactivity, allowing for various chemical transformations, such as condensation reactions. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in the development of agrochemicals or pharmaceuticals. Additionally, the presence of the chlorine atom can enhance lipophilicity and influence the compound's interaction with biological targets. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.

CAS 763109-09-7

5-(4-chlorophenyl)isoxazole-3-carbaldehyde

5-(4-Chlorophenyl)isoxazole-3-carboxaldehyde

Ref: IN-DA003M5O

5-(4-Chlorophenyl)isoxazole-3-carboxaldehyde

Ref: 54-OR1043147

5-(4-Chlorophenyl)isoxazole-3-carboxaldehyde

Ref: 10-F493993