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Structure of 113209-90-8
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This boronate moiety integrates a 4-chloro-5-fluoropyridin-2-yl scaffold with a reactive hydroxymethyl group, enabling direct coupling in cross-coupling protocols. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations, while the bench-stable alcohol functionality simplifies handling and purification.
(4-Chloro-5-fluoropyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its pyridine core supports diverse coupling reactions, while the benzylic alcohol functionality facilitates derivatization via oxidation, protection, or direct substitution. The molecule exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for multi-step synthesis and scale-up applications.
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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: