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Structure of 29124-56-9
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1-(2-Amino-5-bromophenyl)ethanone features a brominated aromatic ring paired with an amino group in the meta position, enabling selective coupling reactions. The acetyl moiety provides a handle for further functionalization, while the electron-donating amine enhances reactivity in electrophilic substitution. This compound serves as a key intermediate in pharmaceutical synthesis and conjugated materials development under standard bench conditions.
1-(2-Amino-5-bromophenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling direct incorporation of both amino and bromo functional groups for downstream cross-coupling and heterocycle formation. Its bench-stable nature and compatibility with palladium-catalyzed reactions facilitate efficient synthesis of complex aromatic scaffolds. Functions as a key intermediate in the construction of bioactive molecules requiring ortho-substituted aniline motifs.
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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: