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Structure of 188774-56-3
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2-Chloro-5-hydroxybenzonitrile features a hydroxyl group flanked by chlorine and nitrile substituents on a benzene ring, enabling dual functionalization in synthetic sequences. This electron-deficient scaffold supports efficient coupling reactions and offers enhanced solubility compared to non-hydroxylated analogs. The molecule’s stability under standard conditions facilitates use in multi-step synthesis, particularly for heterocyclic systems and pharmaceutical intermediates.
2-Chloro-5-hydroxybenzonitrile serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic hydroxyl and nitrile groups. Its ortho-chloro substituent facilitates subsequent cross-coupling reactions, while the hydroxyl group offers opportunities for derivatization or metal complexation. The compound exhibits good bench stability and compatibility with standard purification methods, making it suitable for iterative synthesis workflows in API development.
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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: