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Structure of 473923-97-6
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3-Chloro-5-hydroxybenzonitrile features a hydroxyl group flanked by electron-withdrawing chlorine and nitrile substituents, enabling selective functionalization in synthetic intermediates. This ortho-directed pattern supports efficient derivatization under mild conditions, leveraging the hydroxyl’s reactivity while maintaining stability during purification.
3-Chloro-5-hydroxybenzonitrile serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the hydroxyl and nitrile groups. Its ortho-chloro substituent facilitates palladium-catalyzed cross-coupling reactions, while the phenolic OH allows for derivatization via etherification or esterification. The molecule exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative 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: