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Structure of 1196153-96-4
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2-Chloro-5-fluoropyridin-4-ol features a pyridin-4-ol core with orthogonal halogen substituents at C2 and C5, enabling selective functionalization in late-stage diversification. The electron-deficient ring system facilitates nucleophilic substitution, while the phenolic OH group offers a handle for derivatization under mild conditions. This scaffold exhibits enhanced stability and solubility in polar solvents, streamlining integration into complex synthetic sequences.
2-Chloro-5-fluoropyridin-4-ol serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-halogen and phenolic hydroxyl groups facilitate selective derivatization, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Bench-stable and compatible with common protecting group strategies, it functions reliably in the synthesis of heterocyclic scaffolds and API intermediates.
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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: