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Structure of 887757-25-7
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4-Bromo-3-cyanobenzoic acid features a bromine atom at the 4-position and a cyano group at the 3-position, both strategically positioned relative to the carboxylic acid. This arrangement enables selective coupling reactions in synthetic pathways. The molecule combines electron-withdrawing functionalities with enhanced stability under standard conditions.
4-Bromo-3-cyanobenzoic acid serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to functionalized heterocycles and bioactive scaffolds. Its orthogonal functionality—bromine for cross-coupling, nitrile for transformation to amides or carboxylic acids, and carboxylic acid for derivatization—facilitates modular synthesis. The compound exhibits excellent bench stability and is readily purified by recrystallization, supporting scalable applications in API development and target-oriented synthesis.
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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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: