4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole is a heterocyclic organic compound characterized by the presence of both an oxazole ring and a thiophene moiety. The oxazole ring is a five-membered aromatic structure containing both nitrogen and oxygen, contributing to the compound's potential reactivity and biological activity. The chloromethyl group attached to the oxazole enhances its electrophilic character, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions. The thiophene ring, known for its aromatic properties, adds to the compound's stability and can influence its electronic properties. This compound may exhibit interesting pharmacological activities due to the combination of its functional groups, making it a subject of interest in medicinal chemistry. Additionally, its unique structure may allow for various applications in organic synthesis and materials science. As with many heterocycles, the solubility, stability, and reactivity of this compound can be influenced by the presence of substituents and the overall molecular environment.

4-(chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole

54679-74-2: 4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole is a heterocyclic organic compound characterized by the presence of both an oxazole ring and a thiophene moiety. The oxazole ring is a five-membered aromatic structure containing both nitrogen and oxygen, contributing to the compound's potential reactivity and biological activity. The chloromethyl group attached to the oxazole enhances its electrophilic character, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions. The thiophene ring, known for its aromatic properties, adds to the compound's stability and can influence its electronic properties. This compound may exhibit interesting pharmacological activities due to the combination of its functional groups, making it a subject of interest in medicinal chemistry. Additionally, its unique structure may allow for various applications in organic synthesis and materials science. As with many heterocycles, the solubility, stability, and reactivity of this compound can be influenced by the presence of substituents and the overall molecular environment.

CAS 54679-74-2

4-(chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole

4-(CHLOROMETHYL)-2-THIEN-2-YL-1,3-OXAZOLE

Ref: IN-DA00DQFR

4-(Chloromethyl)-2-(thiophen-2-yl)oxazole

Ref: 54-OR1056178

4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-oxazole

Ref: 3D-ECA67974