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Structure of 53491-80-8
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1-Chloroisoquinoline-4-carbonitrile features a chlorine substituent at the 1-position and a nitrile group at the 4-position of the isoquinoline core. This combination imparts high electrophilicity at the 1-position, enabling selective nucleophilic substitution under mild conditions. The molecule exhibits excellent stability in air and moisture, facilitating handling during synthetic transformations. Its dual functionalization supports direct coupling strategies in medicinal chemistry and materials synthesis.
1-Chloroisoquinoline-4-carbonitrile serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 position via nucleophilic substitution. The chloro group exhibits high reactivity toward amines, thiols, and other nucleophiles under mild conditions, while the nitrile moiety provides a handle for downstream transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with common reaction protocols make it well-suited for modular synthesis of isoquinoline-based scaffolds in drug discovery and process development.
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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: