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Structure of 2407-11-6
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2-Chloro-6-nitrobenzo[d]thiazole features a fused benzothiazole core bearing a chloro group at the 2-position and a nitro group at the 6-position, creating a highly electron-deficient scaffold. This configuration enables efficient coupling in transition-metal-catalyzed cross-coupling reactions, particularly in the synthesis of functionalized heterocycles for pharmaceutical and materials applications. The compound exhibits excellent stability under standard handling conditions.
2-Chloro-6-nitrobenzo[d]thiazole serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of biologically relevant scaffolds. Its chloro group facilitates palladium-catalyzed cross-coupling reactions, while the nitro functionality offers opportunities for selective reduction and subsequent derivatization. The molecule exhibits good bench stability and is compatible with common functional group manipulations, making it well-suited for iterative synthetic strategies in medicinal chemistry and materials science.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: