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Structure of 59236-37-2
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2-Amino-4-chlorobenzaldehyde features a strategically positioned aldehyde group flanked by an electron-donating amino moiety and a chlorine atom, enabling selective reactivity in cross-coupling and condensation reactions. This ortho-substituted scaffold delivers enhanced solubility and stability under standard bench conditions, facilitating efficient integration into complex molecular architectures.
2-Amino-4-chlorobenzaldehyde serves as a versatile building block in the synthesis of pharmaceutical intermediates and functionalized heterocycles. Its ortho-amino and para-chloro substituents enable selective electrophilic substitutions, palladium-catalyzed couplings, and condensation reactions. The aldehyde group facilitates imine formation and Mannich-type reactions, while the amino functionality supports facile derivatization. Bench-stable and amenable to standard purification methods, it functions reliably in multi-step syntheses requiring regioselective transformations.
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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: