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Structure of 502496-36-8
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3-Bromo-5-fluoro-2-methylaniline delivers a strategically functionalized aryl scaffold featuring bromine and fluorine substituents at meta positions relative to the aniline nitrogen, with a methyl group at the ortho position. This combination enables direct coupling in cross-coupling reactions while maintaining stability under standard conditions. The electron-withdrawing halogens enhance reactivity in palladium-catalyzed transformations, facilitating rapid access to complex heterocycles and biaryl architectures.
3-Bromo-5-fluoro-2-methylaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling the construction of substituted anilines via Pd-catalyzed cross-coupling reactions. The ortho-methyl group enhances metabolic stability, while the bromo and fluoro substituents provide complementary sites for further functionalization. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex heterocyclic scaffolds and drug-like molecules.
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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: