4-(Chloromethyl)-2-(2-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 enhances its reactivity, making it useful in various chemical syntheses. The fluorophenyl substituent contributes to its potential biological activity and lipophilicity, which can influence its interaction with biological targets. This compound is typically synthesized through multi-step organic reactions, involving the formation of the oxazole ring and subsequent introduction of the chloromethyl and fluorophenyl groups. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of new drugs, due to the presence of functional groups that can participate in various chemical reactions. Additionally, the compound's properties, such as solubility, stability, and reactivity, can be influenced by the substituents on the oxazole ring, making it a subject of interest in medicinal chemistry and material science. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

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

671215-76-2: 4-(Chloromethyl)-2-(2-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 enhances its reactivity, making it useful in various chemical syntheses. The fluorophenyl substituent contributes to its potential biological activity and lipophilicity, which can influence its interaction with biological targets. This compound is typically synthesized through multi-step organic reactions, involving the formation of the oxazole ring and subsequent introduction of the chloromethyl and fluorophenyl groups. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of new drugs, due to the presence of functional groups that can participate in various chemical reactions. Additionally, the compound's properties, such as solubility, stability, and reactivity, can be influenced by the substituents on the oxazole ring, making it a subject of interest in medicinal chemistry and material science. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

4-(Chloromethyl)-2-(2-fluorophenyl)-5-methyloxazole

<p>4-(Chloromethyl)-2-(2-fluorophenyl)-5-methyloxazole</p>

CAS 671215-76-2

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

4-(Chloromethyl)-2-(2-fluorophenyl)-5-methyloxazole

Ref: IN-DA006LGE

4-(Chloromethyl)-2-(2-fluorophenyl)-5-methyloxazole

Ref: 54-PC1005107

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

Ref: 10-F308643