Methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. The presence of a bromine atom at the 2-position and an isopropyl group at the 5-position contributes to its unique reactivity and physical properties. This compound features a carboxylate ester functional group, which enhances its solubility in organic solvents and may influence its biological activity. The methyl ester group can participate in various chemical reactions, such as hydrolysis or transesterification. Methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate is of interest in medicinal chemistry and agrochemicals, potentially serving as a precursor for the synthesis of biologically active molecules. Its specific applications and reactivity can be influenced by the presence of the bromine atom, which can act as a leaving group in nucleophilic substitution reactions. Overall, this compound exemplifies the diverse chemistry associated with thiazole derivatives.

methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate

81569-28-0: Methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. The presence of a bromine atom at the 2-position and an isopropyl group at the 5-position contributes to its unique reactivity and physical properties. This compound features a carboxylate ester functional group, which enhances its solubility in organic solvents and may influence its biological activity. The methyl ester group can participate in various chemical reactions, such as hydrolysis or transesterification. Methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate is of interest in medicinal chemistry and agrochemicals, potentially serving as a precursor for the synthesis of biologically active molecules. Its specific applications and reactivity can be influenced by the presence of the bromine atom, which can act as a leaving group in nucleophilic substitution reactions. Overall, this compound exemplifies the diverse chemistry associated with thiazole derivatives.

CAS 81569-28-0

methyl 2-bromo-5-(1-methylethyl)-1,3-thiazole-4-carboxylate

Methyl 2-bromo-5-isopropylthiazole-4-carboxylate

Ref: IN-DA00G83X

Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate

Ref: 54-OR15559

Methyl 2-bromo-5-isopropylthiazole-4-carboxylate

Ref: 10-F231980