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Structure of 2420-16-8
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3-Chloro-4-hydroxybenzaldehyde features a hydroxyl group adjacent to a chlorine-substituted benzene ring, enabling strong hydrogen bonding and enhanced solubility in polar solvents. This electron-deficient aldehyde integrates readily into coupling reactions, serving as a key building block for bioactive molecules and functional materials.
3-Chloro-4-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinoline derivatives, and other heterocyclic scaffolds. The aldehyde group facilitates nucleophilic addition and condensation reactions, while the phenolic hydroxyl and chloro substituents offer orthogonal reactivity for selective functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling and cyclization protocols.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H317-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P272-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: