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Structure of 72635-78-0
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3-Amino-4-bromobenzonitrile features a bromine atom at the para position relative to the nitrile group, enabling direct functionalization in cross-coupling reactions. The electron-donating amino group enhances reactivity at the adjacent ring position, while the nitrile moiety provides a versatile handle for further derivatization. This compound serves as a key intermediate in the synthesis of pharmaceuticals and functional materials.
3-Amino-4-bromobenzonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its compatible bromo and nitrile functionalities. The amino group facilitates further derivatization via acylation or diazotization, while the nitrile remains stable under standard reaction conditions. Its bench-stable solid form simplifies handling and purification, making it well-suited for multi-step synthesis of heterocyclic scaffolds and API intermediates.
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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: