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Structure of 16582-59-5
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4,6-Dichlorobenzo[d]thiazol-2-amine features a rigid, electron-deficient heterocyclic core that integrates readily into bioactive scaffolds. The dichloro substitution pattern enhances metabolic stability and facilitates directed functionalization. This bench-stable compound serves as a key building block for pharmaceutical intermediates and advanced materials, offering predictable reactivity in coupling processes under standard conditions.
4,6-Dichlorobenzo[d]thiazol-2-amine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its dual chloro substituents provide orthogonal reactivity for sequential functionalization, while the thiazole nitrogen enhances solubility and stability under standard reaction conditions. This compound facilitates rapid diversification in medicinal chemistry workflows and is well-suited for scale-up in API intermediate development.
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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: