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Structure of 2942-22-5
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2-Chloro-7-nitro-1,3-benzothiazole features a fused heterocyclic core bearing both chloro and nitro substituents at distinct positions, enabling selective functionalization in synthetic routes. The electron-deficient aromatic system enhances reactivity in nucleophilic substitution processes, while the bench-stable crystalline form facilitates handling under standard conditions.
2-Chloro-7-nitro-1,3-benzothiazole serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the 2-position via palladium-catalyzed cross-coupling. The electron-deficient benzothiazole core enhances reactivity in nucleophilic substitution, while the ortho-chloro and meta-nitro groups provide orthogonal handles for sequential transformations. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to substituted benzothiazoles relevant to medicinal chemistry and agrochemical research.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: