3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carbaldehyde is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This specific compound features a dichlorophenyl group, indicating the presence of two chlorine atoms on the phenyl ring, which can significantly influence its reactivity and biological activity. The methyl group at the 5-position of the isoxazole ring adds to its structural complexity. The aldehyde functional group at the 4-position is notable for its reactivity, particularly in condensation reactions and as a potential electrophile in various organic transformations. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its unique structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of halogen substituents can enhance lipophilicity and influence the compound's interaction with biological targets. Overall, this compound exemplifies the diverse chemistry associated with isoxazole derivatives.

3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carbaldehyde

849060-70-4: 3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carbaldehyde is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This specific compound features a dichlorophenyl group, indicating the presence of two chlorine atoms on the phenyl ring, which can significantly influence its reactivity and biological activity. The methyl group at the 5-position of the isoxazole ring adds to its structural complexity. The aldehyde functional group at the 4-position is notable for its reactivity, particularly in condensation reactions and as a potential electrophile in various organic transformations. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its unique structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of halogen substituents can enhance lipophilicity and influence the compound's interaction with biological targets. Overall, this compound exemplifies the diverse chemistry associated with isoxazole derivatives.

CAS 849060-70-4

3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carbaldehyde

3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carbaldehyde

Ref: IN-DA004VM8

3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carbaldehyde

Ref: 54-OR322551

3-(2,6-DICHLOROPHENYL)-5-METHYLISOXAZOLE-4-CARBALDEHYDE

Ref: 10-F813190