4-(Bromomethyl)-1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole is a chemical compound characterized by its complex structure, which includes a pyrazole ring substituted with various functional groups. The presence of a bromomethyl group indicates a potential for reactivity, particularly in nucleophilic substitution reactions. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and influencing the compound's biological activity. The phenoxy group contributes to the compound's overall stability and can affect its solubility in organic solvents. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in agrochemicals or pharmaceuticals, particularly in the development of new therapeutic agents. The CAS number 912569-72-3 provides a unique identifier for this substance, facilitating its identification in chemical databases and literature. Overall, the combination of these substituents suggests a compound with diverse chemical reactivity and potential applications in various fields.

4-(bromomethyl)-1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole

912569-72-3: 4-(Bromomethyl)-1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole is a chemical compound characterized by its complex structure, which includes a pyrazole ring substituted with various functional groups. The presence of a bromomethyl group indicates a potential for reactivity, particularly in nucleophilic substitution reactions. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and influencing the compound's biological activity. The phenoxy group contributes to the compound's overall stability and can affect its solubility in organic solvents. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in agrochemicals or pharmaceuticals, particularly in the development of new therapeutic agents. The CAS number 912569-72-3 provides a unique identifier for this substance, facilitating its identification in chemical databases and literature. Overall, the combination of these substituents suggests a compound with diverse chemical reactivity and potential applications in various fields.

CAS 912569-72-3

4-(bromomethyl)-1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole

4-(Bromomethyl)-1-methyl-5-phenoxy-3-(trifluoromethyl)-1H-pyrazole

Ref: 54-PC3229