5-Bromo-4-methyl-1,3-thiazole is a heterocyclic organic compound characterized by its thiazole ring, which contains both sulfur and nitrogen atoms. The presence of a bromine atom at the 5-position and a methyl group at the 4-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It exhibits moderate solubility in organic solvents, while its reactivity can be influenced by the electron-withdrawing nature of the bromine atom. The thiazole ring system is known for its role in various biochemical processes, making derivatives of this compound of interest in medicinal chemistry. Additionally, 5-Bromo-4-methyl-1,3-thiazole can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, which are valuable in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

5-Bromo-4-methyl-1,3-thiazole

111600-83-0: Thiazole, 5-Bromo-4-Methyl-, 5-Bromo-4-methyl-thiazole

5-Bromo-4-methylthiazole

5-Bromo-4-methylthiazole is an electron-deficient electrophilic compound that can undergo nucleophilic attack. It is synthesized by the reaction of a benzene derivative with methyl iodide in the presence of a palladium complex as a catalyst. 5-Bromo-4-methylthiazole has been used to study nucleophilic attack, electron donation, and electronegativity. This heterocycle has also been used to study oxidative degradation in nature.

CAS 111600-83-0: 5-Bromo-4-methyl-1,3-thiazole

5-Bromo-4-methyl-1,3-thiazole

Ref: 54-OR18109

5-Bromo-4-methylthiazole

Ref: IN-DA003485

5-Bromo-4-methylthiazole

Ref: 10-F323619

5-Bromo-4-methylthiazole

Ref: 3D-FB10679