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Structure of 2605-14-3
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2-Chloro-6-methoxybenzo[d]thiazole features a fused benzothiazole core with strategically positioned electron-withdrawing chlorine and electron-donating methoxy groups, enhancing its reactivity in cross-coupling and electrophilic substitution reactions. This bench-stable heterocycle integrates readily into complex molecular architectures, offering predictable regioselectivity under standard conditions.
2-Chloro-6-methoxybenzo[d]thiazole serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically relevant heterocyclic scaffolds. The chloro group facilitates palladium-catalyzed cross-coupling reactions, while the methoxy substituent enhances solubility and modulates electronic properties. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for synthesizing complex molecules in drug discovery 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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: