4-(Bromomethyl)-2-methyl-1,3-thiazole is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features a bromomethyl group (-CH2Br) at the 4-position and a methyl group (-CH3) at the 2-position of the thiazole ring. It is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. The presence of the bromine atom contributes to its reactivity, making it useful in various chemical synthesis applications, particularly in the development of pharmaceuticals and agrochemicals. The thiazole moiety is known for its biological activity, and compounds containing this structure often exhibit antimicrobial, antifungal, or anticancer properties. Additionally, 4-(bromomethyl)-2-methyl-1,3-thiazole can undergo nucleophilic substitution reactions due to the electrophilic nature of the bromomethyl group, allowing for further functionalization and derivatization in organic synthesis.

4-(bromomethyl)-2-methyl-1,3-thiazole

74704-39-5: 4-(Bromomethyl)-2-methyl-1,3-thiazole is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features a bromomethyl group (-CH2Br) at the 4-position and a methyl group (-CH3) at the 2-position of the thiazole ring. It is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. The presence of the bromine atom contributes to its reactivity, making it useful in various chemical synthesis applications, particularly in the development of pharmaceuticals and agrochemicals. The thiazole moiety is known for its biological activity, and compounds containing this structure often exhibit antimicrobial, antifungal, or anticancer properties. Additionally, 4-(bromomethyl)-2-methyl-1,3-thiazole can undergo nucleophilic substitution reactions due to the electrophilic nature of the bromomethyl group, allowing for further functionalization and derivatization in organic synthesis.

CAS 74704-39-5

4-(bromomethyl)-2-methyl-1,3-thiazole

THIAZOLE, 4-(BROMOMETHYL)-2-METHYL-

Ref: IN-DA005A2T