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Structure of 22246-13-5
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6-Amino-3,4-dihydroquinoline-2(1H)-one features a fused heterocyclic core with a strategically positioned amino group enabling direct functionalization. This scaffold delivers enhanced solubility and reactivity in synthetic transformations, particularly useful in medicinal chemistry for constructing bioactive analogs. The compound exhibits bench-stable handling under standard conditions and integrates readily into multi-step synthesis workflows.
6-Amino-3,4-dihydroquinoline-2(1H)-one serves as a versatile scaffold for medicinal chemistry and synthetic intermediate development. Its dual functionality—amine and carbonyl groups—enables straightforward derivatization via amidation, alkylation, or coupling reactions. The compound exhibits good bench stability and facilitates access to quinoline-based heterocycles relevant in drug discovery programs.
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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: