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Structure of 1427433-65-5
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6-Bromo-4-fluoro-2-methylbenzo[d]thiazole features a fused heterocyclic core with strategically positioned halogen and methyl substituents. This electron-deficient scaffold enables efficient coupling in cross-coupling reactions, particularly Pd-catalyzed variants. The bromine atom serves as a high-reactivity handle for C–C bond formation, while the fluorine enhances metabolic stability and modulates electronic properties. Bench-stable under standard conditions, it integrates readily into complex molecular architectures.
6-Bromo-4-fluoro-2-methylbenzo[d]thiazole serves as a versatile building block in the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its orthogonal halogenation pattern enables selective cross-coupling reactions, while the methyl group provides a handle for further functionalization. The molecule exhibits excellent bench stability and compatibility with palladium-catalyzed transformations, facilitating efficient access to complex scaffolds in medicinal chemistry and process development 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: