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Structure of 3336-49-0
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isoquinolin-4-ol delivers a rigid, electron-rich heterocyclic scaffold ideal for constructing bioactive molecules. The phenolic hydroxyl group enables direct functionalization or metal chelation, while the fused ring system confers enhanced stability and planarity. This compound serves as a key intermediate in alkaloid synthesis and medicinal chemistry campaigns requiring a polar, aromatic core with defined hydrogen-bonding capacity.
isoquinolin-4-ol serves as a versatile heterocyclic building block in medicinal chemistry, enabling direct access to isoquinoline-based scaffolds prevalent in natural products and bioactive molecules. Its phenolic hydroxyl group offers moderate stability and facilitates selective derivatization via etherification or metal-catalyzed coupling reactions. The compound functions as a key intermediate in the synthesis of alkaloids and exhibits favorable handling characteristics for bench-scale applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: