5-Methyl-1,3-benzothiazole is an organic compound characterized by its fused benzene and thiazole rings, which contribute to its aromatic properties. It typically appears as a yellow to light brown solid and has a distinct odor. The presence of the methyl group at the 5-position of the benzothiazole structure influences its chemical reactivity and solubility. This compound is known for its applications in various fields, including pharmaceuticals, agrochemicals, and as a precursor in the synthesis of other organic compounds. It exhibits moderate stability under standard conditions but may undergo reactions typical of thiazole derivatives, such as electrophilic substitution. Additionally, 5-methyl-1,3-benzothiazole can participate in various chemical reactions, including nucleophilic attacks and oxidation processes. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, its unique structure and properties make it a valuable compound in chemical research and industrial applications.

5-methyl-1,3-benzothiazole

2942-16-7: 5-Methyl-1,3-benzothiazole is an organic compound characterized by its fused benzene and thiazole rings, which contribute to its aromatic properties. It typically appears as a yellow to light brown solid and has a distinct odor. The presence of the methyl group at the 5-position of the benzothiazole structure influences its chemical reactivity and solubility. This compound is known for its applications in various fields, including pharmaceuticals, agrochemicals, and as a precursor in the synthesis of other organic compounds. It exhibits moderate stability under standard conditions but may undergo reactions typical of thiazole derivatives, such as electrophilic substitution. Additionally, 5-methyl-1,3-benzothiazole can participate in various chemical reactions, including nucleophilic attacks and oxidation processes. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, its unique structure and properties make it a valuable compound in chemical research and industrial applications.

CAS 2942-16-7

5-methyl-1,3-benzothiazole

Benzothiazole, 5-methyl-

Ref: IN-DA002YBU

5-Methylbenzo[d]thiazole

Ref: 54-OR82329

5-Methylbenzo[d]thiazole

Ref: 10-F242309