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Structure of 727736-70-1
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6-Chloro-3-hydroxypicolinonitrile features a strategically positioned hydroxyl group and nitrile moiety on a pyridine scaffold, enabling direct integration into heterocyclic syntheses. The chlorine substituent provides a reactive handle for palladium-catalyzed coupling reactions. This bench-stable compound serves as a key intermediate in the development of bioactive nitrogen-containing architectures.
6-Chloro-3-hydroxypicolinonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds. The molecule combines a reactive chloro group for nucleophilic substitution and a hydroxyl function amenable to derivatization, while the nitrile moiety supports downstream transformations such as amidation or hydrolysis. Its bench-stable nature and compatibility with standard coupling protocols facilitate integration into multi-step syntheses of bioactive heterocycles.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: