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Structure of 1395493-30-7
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Methyl 2-amino-4-bromo-5-fluorobenzoate features a uniquely functionalized aromatic core with complementary electron-donating (amino) and electron-withdrawing (bromo, fluoro) substituents. This combination enables precise tuning of reactivity in cross-coupling and electrophilic substitution processes. The methyl ester group provides a stable handle for subsequent derivatization, while the bench-stable nature facilitates handling under standard conditions.
Methyl 2-amino-4-bromo-5-fluorobenzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. The molecule combines ortho-directed reactivity from the amino group with complementary halogenation sites for palladium-catalyzed cross-coupling. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient purification and scalable transformations in multi-step syntheses.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: