4-Chloro-1,3-thiazol-2-amine is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of a chlorine atom at the 4-position and an amino group at the 2-position contributes to its reactivity and potential applications in various chemical reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. It is often used in the synthesis of pharmaceuticals and agrochemicals, as well as in research settings for its biological activity. The thiazole moiety is known for its role in various biological processes, making 4-chloro-1,3-thiazol-2-amine of interest in medicinal chemistry. Safety data should be consulted for handling, as with many chemical substances, it may pose health risks if not managed properly. Overall, its unique structure and functional groups make it a valuable compound in organic synthesis and medicinal applications.

4-chloro-1,3-thiazol-2-amine

52107-46-7: 4-Chloro-1,3-thiazol-2-amine is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of a chlorine atom at the 4-position and an amino group at the 2-position contributes to its reactivity and potential applications in various chemical reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. It is often used in the synthesis of pharmaceuticals and agrochemicals, as well as in research settings for its biological activity. The thiazole moiety is known for its role in various biological processes, making 4-chloro-1,3-thiazol-2-amine of interest in medicinal chemistry. Safety data should be consulted for handling, as with many chemical substances, it may pose health risks if not managed properly. Overall, its unique structure and functional groups make it a valuable compound in organic synthesis and medicinal applications.

CAS 52107-46-7

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