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Structure of 2941-48-2
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2,5-Dichlorobenzo[d]thiazole features a rigid, electron-deficient heterocyclic core that integrates seamlessly into pharmaceutical and materials synthesis. The ortho-chlorine substituents enhance reactivity in electrophilic substitution while maintaining stability under standard conditions. This compound serves as a key scaffold for bioactive molecules and functional polymers.
2,5-Dichlorobenzo[d]thiazole serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of complex scaffolds via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern provides orthogonal reactivity for sequential functionalization, while the benzo[d]thiazole core offers enhanced stability and favorable electronic properties for medicinal chemistry applications. Its bench-stable nature and compatibility with standard synthetic protocols facilitate straightforward purification and integration into multi-step sequences.
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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: