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Structure of 174302-46-6
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7-Aminoisoquinolin-1(2H)-one delivers a nitrogen-rich heterocyclic scaffold with enhanced solubility and stability under standard conditions. This electron-donating amino group flanks a lactam core, enabling direct integration into bioactive molecules. The structure supports efficient coupling reactions and serves as a key building block in medicinal chemistry for kinase inhibitors and fluorescent probes.
7-Aminoisoquinolin-1(2H)-one serves as a versatile scaffold for medicinal chemistry and materials science, enabling direct functionalization at the amino and carbonyl positions. Its inherent stability under standard reaction conditions facilitates coupling reactions, derivatization, and incorporation into heterocyclic frameworks. The compound functions as a key building block in the synthesis of bioactive molecules and advanced organic semiconductors, offering excellent solubility and predictable reactivity in amide bond formation and transition-metal-catalyzed transformations.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: