Methyl 2-chloro-1,3-benzothiazole-6-carboxylate is an organic compound characterized by its benzothiazole structure, which consists of a benzene ring fused to a thiazole ring. This compound features a carboxylate group, which contributes to its reactivity and solubility in polar solvents. The presence of a chlorine atom at the 2-position of the benzothiazole ring enhances its electrophilic properties, making it useful in various chemical reactions. Methyl 2-chloro-1,3-benzothiazole-6-carboxylate is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. It is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to participate in nucleophilic substitution reactions. Additionally, its unique structure may impart specific biological activities, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

methyl 2-chloro-1,3-benzothiazole-6-carboxylate

90792-69-1: 6-Benzothiazolecarboxylic Acid, 2-Chloro-, Methyl Ester

Methyl 2-chlorobenzo[d]thiazole-6-carboxylate

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CAS 90792-69-1: methyl 2-chloro-1,3-benzothiazole-6-carboxylate

Methyl 2-chlorobenzo[d]thiazole-6-carboxylate

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methyl 2-chlorobenzo[d]thiazole-6-carboxylate

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methyl 2-chlorobenzo[d]thiazole-6-carboxylate

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Methyl 2-chlorobenzo[d]thiazole-6-carboxylate

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