4-(Chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole is a heterocyclic organic compound characterized by its oxazole ring, which contains both nitrogen and oxygen atoms. The presence of a chloromethyl group and a 4-fluorophenyl substituent contributes to its unique chemical properties. This compound typically exhibits moderate to high lipophilicity due to the aromatic fluorophenyl group, which can influence its solubility and reactivity. The oxazole ring is known for its potential biological activity, making such compounds of interest in medicinal chemistry. Additionally, the chloromethyl group can serve as a reactive site for further chemical modifications, enhancing its utility in synthetic applications. The compound's molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Its specific reactivity and interactions would depend on the functional groups present and the overall molecular conformation. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity associated with halogenated compounds.

4-(chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole

625826-69-9: 4-(Chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole is a heterocyclic organic compound characterized by its oxazole ring, which contains both nitrogen and oxygen atoms. The presence of a chloromethyl group and a 4-fluorophenyl substituent contributes to its unique chemical properties. This compound typically exhibits moderate to high lipophilicity due to the aromatic fluorophenyl group, which can influence its solubility and reactivity. The oxazole ring is known for its potential biological activity, making such compounds of interest in medicinal chemistry. Additionally, the chloromethyl group can serve as a reactive site for further chemical modifications, enhancing its utility in synthetic applications. The compound's molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Its specific reactivity and interactions would depend on the functional groups present and the overall molecular conformation. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity associated with halogenated compounds.

CAS 625826-69-9

4-(chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole

4-Chloromethyl-2-(4-fluoro-phenyl)-5-methyl-oxazole

Ref: IN-DA00E9YG

4-(Chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole

Ref: 54-PC107440

4-(chloromethyl)-2-(4-fluorophenyl)-5-methyl-1,3-oxazole

Ref: 10-F308645