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Structure of 13669-51-7
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Quinolin-3-ylmethanol features a rigid quinoline core linked to a primary alcohol, enabling direct functionalization in medicinal chemistry. This bench-stable scaffold integrates readily into bioactive molecules, serving as a key intermediate for kinase inhibitors and fluorescent probes.
Quinolin-3-ylmethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to quinoline-based scaffolds through oxidation, substitution, and coupling reactions. Its bench-stable nature and compatibility with common functional groups facilitate straightforward purification and integration into multi-step syntheses. The alcohol functionality supports direct derivatization or activation for C–C and C–heteroatom bond formation, making it a practical choice for constructing bioactive heterocycles and lead optimization campaigns.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: