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Structure of 216099-46-6
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6-Aminoisoquinolin-1(2H)-one features a fused heterocyclic core with a strategically positioned amino group, enabling direct functionalization in medicinal chemistry. This scaffold integrates readily into bioactive molecules due to its planar structure and hydrogen-bonding capacity. The compound exhibits enhanced solubility and stability under standard conditions, facilitating use in synthetic workflows and target-oriented drug discovery.
6-Aminoisoquinolin-1(2H)-one serves as a versatile scaffold for constructing biologically relevant heterocycles and pharmaceutical intermediates. The amino group enables direct functionalization, while the lactam carbonyl offers sites for derivatization or metal coordination. Its stability under standard reaction conditions facilitates use in cross-coupling, acylation, and cyclization protocols. This compound functions effectively as a building block in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active agents.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: