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Structure of 101253-50-3
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5-Chloro-2-methylbenzo[d]thiazol-6-amine features a fused benzothiazole core with strategically positioned chloro and methyl substituents, enhancing electronic modulation and metabolic stability. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds, offering improved solubility and robustness under standard bench conditions.
5-Chloro-2-methylbenzo[d]thiazol-6-amine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The chloro group at C5 facilitates functionalization, while the aniline functionality supports derivatization under mild conditions. Bench-stable and readily purified by recrystallization, it functions reliably in medicinal chemistry campaigns requiring ortho-substituted thiazole cores.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: