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Structure of 582303-10-4
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This bench-stable (2,6-dimethylpyridin-3-yl)methanol features a sterically hindered pyridine core that enhances regioselectivity in coupling reactions. The primary alcohol moiety enables straightforward derivatization, while the electron-rich aromatic system supports efficient metal coordination. Ideal for constructing functionalized heterocyclic scaffolds in medicinal chemistry and catalysis.
(2,6-Dimethylpyridin-3-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds. Its benzylic alcohol functionality facilitates straightforward derivatization via oxidation, protection, or coupling reactions. The 2,6-dimethyl substitution enhances stability and modulates electronic properties, while the pyridine ring provides a robust platform for metal-catalyzed transformations. This compound functions reliably in standard synthetic workflows, offering excellent bench stability and compatibility with common functional groups.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: