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Structure of 20358-00-3
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2-Amino-5-chlorobenzothiazole features a fused heterocyclic core with complementary electron-donating and electron-withdrawing substituents, enabling robust participation in transition-metal-catalyzed cross-coupling reactions. This bench-stable compound integrates efficiently into complex molecular architectures under standard conditions.
2-Amino-5-chlorobenzothiazole serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its amino and chloro substituents enable diverse functionalization via palladium-catalyzed cross-coupling, nucleophilic substitution, and electrophilic aromatic substitution reactions. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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-H312-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: