4-(Chloromethyl)-2-(thiophen-3-yl)-1,3-thiazole is a heterocyclic organic compound characterized by its thiazole and thiophene rings, which contribute to its unique chemical properties. The presence of a chloromethyl group enhances its reactivity, making it a potential intermediate in organic synthesis. This compound typically exhibits moderate to high solubility in polar organic solvents, while its solid-state properties may include crystalline or amorphous forms depending on the conditions of synthesis. The thiazole ring provides a site for potential nucleophilic attack, while the thiophene moiety can participate in π-π stacking interactions, influencing its electronic properties. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability under standard laboratory conditions is generally good, although it should be handled with care due to the presence of the chloromethyl group, which can be reactive. Overall, 4-(chloromethyl)-2-(thiophen-3-yl)-1,3-thiazole is a versatile compound with applications in various fields, including medicinal chemistry and materials science.

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

54747-64-7: 4-(Chloromethyl)-2-(thiophen-3-yl)-1,3-thiazole is a heterocyclic organic compound characterized by its thiazole and thiophene rings, which contribute to its unique chemical properties. The presence of a chloromethyl group enhances its reactivity, making it a potential intermediate in organic synthesis. This compound typically exhibits moderate to high solubility in polar organic solvents, while its solid-state properties may include crystalline or amorphous forms depending on the conditions of synthesis. The thiazole ring provides a site for potential nucleophilic attack, while the thiophene moiety can participate in π-π stacking interactions, influencing its electronic properties. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability under standard laboratory conditions is generally good, although it should be handled with care due to the presence of the chloromethyl group, which can be reactive. Overall, 4-(chloromethyl)-2-(thiophen-3-yl)-1,3-thiazole is a versatile compound with applications in various fields, including medicinal chemistry and materials science.

CAS 54747-64-7

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

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

Ref: 3D-ECA74764