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Structure of 131002-09-0
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6-Chloroisoquinolin-1(2H)-one is a heterocyclic scaffold featuring a chlorine substituent at the 6-position, enhancing electrophilicity at the C6 carbon. This electron-deficient core facilitates nucleophilic aromatic substitution and serves as a key building block in medicinal chemistry for targeted drug discovery. The lactam functionality provides rigidity and hydrogen-bonding capacity, improving binding affinity and metabolic stability.
6-Chloroisoquinolin-1(2H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C6 position via palladium-catalyzed cross-coupling. Its stability under standard reaction conditions and compatibility with diverse nucleophiles facilitate efficient access to substituted isoquinolinones. The molecule functions as a key scaffold for constructing bioactive heterocycles and supports orthogonal transformations in multi-step synthesis.
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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: