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Structure of 17797-12-5
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This bench-stable arylamine features a sterically hindered tertiary amine core paired with a para-brominated phenyl ring. The bromo substituent enables direct functionalization in cross-coupling reactions, while the bulky isopropyl group enhances metabolic stability. Ideal for constructing bioactive scaffolds and pharmaceutical intermediates.
2-(4-Bromophenyl)propan-2-amine serves as a versatile building block in medicinal chemistry, enabling the synthesis of aryl-substituted tertiary amines via palladium-catalyzed cross-coupling reactions. Its bench-stable, sterically protected amine functionality offers excellent functional group tolerance and facilitates straightforward purification, making it well-suited for modular construction of bioactive 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: