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Structure of 1197-05-3
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1-(3-Aminophenyl)propan-1-one features a conjugated aryl ketone scaffold with a para-amino substituent, enabling direct incorporation into bioactive molecule scaffolds. The amine group facilitates derivatization via acylation or coupling reactions, while the ketone offers electrophilic reactivity for nucleophilic addition. This dual functionality supports rapid access to pharmaceutical intermediates and functionalized aromatic systems under standard conditions.
1-(3-Aminophenyl)propan-1-one serves as a versatile building block for pharmaceutical intermediates, enabling efficient construction of biologically relevant scaffolds. Its amine and ketone functionalities offer orthogonal reactivity for coupling, cyclization, and derivatization under standard conditions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: