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Structure of 221050-96-0
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Isoquinoline-7-carboxylic acid delivers a rigid, electron-deficient heteroaromatic scaffold ideal for constructing bioactive molecules. This bench-stable derivative features a carboxylic acid group at the C7 position, enabling direct conjugation or derivatization in medicinal chemistry campaigns. Its planar structure supports π-stacking interactions in target binding environments.
Isoquinoline-7-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into bioactive heterocycles due to its inherent rigidity and defined polarity. The carboxylic acid group facilitates straightforward derivatization—via amide coupling, esterification, or activation for nucleophilic substitution—while the isoquinoline core provides a stable scaffold for structure-activity studies. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses targeting alkaloid analogs and kinase inhibitors.
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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: