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Structure of 61613-22-7
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2-Bromo-N-phenylaniline features a bromine substituent at the ortho position relative to the aniline nitrogen, enhancing electrophilic reactivity in cross-coupling processes. The N-phenyl group imparts steric and electronic modulation, improving stability under standard conditions while enabling precise functionalization in pharmaceutical and materials synthesis.
2-Bromo-N-phenylaniline serves as a versatile building block in cross-coupling chemistry, enabling efficient palladium-catalyzed C–N and C–C bond formations. Its bromine substituent provides high reactivity in Suzuki, Stille, and Buchwald–Hartwig reactions, while the aniline functionality offers moderate nucleophilicity and compatibility with common protecting groups. The compound exhibits excellent bench stability and is readily purified by recrystallization or column chromatography, facilitating its use in the synthesis of biaryl scaffolds, pharmaceutical intermediates, and functionalized heterocycles.
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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: