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Structure of 214055-12-6
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(5-Chloro-3-fluoropyridin-2-yl)methanol features a pyridine core functionalized with chlorine and fluorine at the 5- and 3-positions, respectively, and a reactive methanol group at the 2-position. This trifunctional scaffold enables direct incorporation into bioactive molecules, offering enhanced metabolic stability and targeted electronic modulation in pharmaceutical development.
(5-Chloro-3-fluoropyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated pyridine scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and coupling reactions with broad functional group tolerance. The molecule exhibits bench stability and is readily purified by standard chromatographic methods, making it well-suited for multi-step synthesis and process development in API research.
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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: