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Structure of 5407-51-2
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1,3-Benzothiazole-2,6-diamine features a fused benzene-thiazole core with two strategically positioned primary amine groups. This electron-rich scaffold enables direct integration into functionalized polymers and bioconjugation workflows. The diamine moiety enhances solubility in polar solvents and facilitates metal coordination in catalytic systems. Bench-stable under ambient conditions, it serves as a robust building block for advanced materials and pharmaceutical intermediates.
1,3-Benzothiazole-2,6-diamine serves as a versatile heterocyclic building block for the synthesis of pharmaceutically relevant scaffolds. Its dual amine functionality enables straightforward derivatization via amidation, alkylation, and coupling reactions. The rigid benzothiazole core imparts metabolic stability and favorable binding interactions, making it valuable in medicinal chemistry campaigns targeting kinase inhibitors and CNS agents. Bench-stable and readily purified by recrystallization, it functions effectively in standard peptide and small-molecule synthesis workflows.
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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-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: