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Structure of 2420-26-0
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4-Chloro-2-hydroxybenzaldehyde features a hydroxyl group ortho to the aldehyde, enabling intramolecular hydrogen bonding that enhances stability and influences reactivity. This electron-deficient aromatic scaffold integrates readily into synthetic pathways for bioactive molecules, particularly in pharmaceutical intermediates and ligand design.
4-Chloro-2-hydroxybenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of bioactive heterocycles and pharmaceutical intermediates. Its ortho-hydroxyl group facilitates intramolecular cyclization, while the aldehyde functionality supports nucleophilic addition and condensation reactions. The electron-withdrawing chlorine substituent enhances reactivity in electrophilic substitution and improves metabolic stability in downstream drug candidates. This compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for routine laboratory-scale synthesis and process 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: