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Structure of 19493-45-9
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3-Chloroisoquinoline serves as a pivotal building block in medicinal chemistry, offering a rigid, electron-deficient heterocyclic scaffold. This chlorinated isoquinoline integrates readily into diverse synthetic pathways, enabling efficient access to bioactive compounds through cross-coupling and nucleophilic substitution reactions. Its bench-stable nature supports reliable handling under standard conditions.
3-Chloroisoquinoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C3 position via palladium-catalyzed cross-coupling reactions. Its moderate electrophilicity and bench stability facilitate incorporation into diverse heterocyclic scaffolds, particularly in the synthesis of kinase inhibitors and CNS-targeted compounds. The chlorine atom provides a reliable handle for further derivatization under standard conditions.
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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: