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Structure of 1227602-31-4
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(6-Chloro-5-methoxypyridin-2-yl)methanol features a pyridine core functionalized with chlorine and methoxy groups at positions 6 and 5, respectively, and a reactive hydroxymethyl substituent at position 2. This configuration enables direct coupling in cross-coupling reactions or derivatization via oxidation to the aldehyde. The molecule exhibits good solubility in common organic solvents and stability under standard bench conditions, facilitating its use in synthetic workflows for pharmaceutical intermediates and agrochemicals.
(6-Chloro-5-methoxypyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through nucleophilic substitution and coupling reactions. Its chloro group facilitates C–H functionalization, while the methoxy and hydroxymethyl functionalities provide orthogonal handles for further derivatization. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns and API intermediate development.
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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: