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Structure of 131747-60-9
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This fluorinated pyridine derivative features a reactive hydroxymethyl group at the 4-position, enabling straightforward functionalization. The electron-deficient pyridine ring enhances electrophilic reactivity, while the fluorine substituent imparts metabolic stability and modulates electronic properties. Ideal for medicinal chemistry applications requiring polar, rigid scaffolds with tunable solubility and bioavailability.
(2-Fluoropyridin-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient incorporation of fluorinated pyridine motifs into target molecules. Its benzylic alcohol functionality facilitates straightforward derivatization—such as oxidation to the carboxylic acid or activation for coupling reactions—while maintaining compatibility with diverse reaction conditions. The molecule exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for use in multi-step synthesis and API development workflows.
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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: