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Structure of 1279865-14-3
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2-Amino-4-bromo-6-fluorobenzonitrile features a strategically positioned electron-deficient aromatic core with orthogonal halogen and nitrile functionalities. This configuration enables direct coupling in cross-coupling reactions, while the amino group supports further derivatization. The compound exhibits robust stability under standard conditions, facilitating reliable integration into complex synthetic sequences.
2-Amino-4-bromo-6-fluorobenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The amino group facilitates downstream derivatization via acylation or electrophilic substitution, while the nitrile functions as a handle for hydrolysis or reduction. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of complex heterocyclic scaffolds and functionalized aromatic systems.
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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: