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Structure of 5568-33-2
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2-Chloro-4-nitrobenzaldehyde features a conjugated aldehyde group flanked by electron-withdrawing chlorine and nitro substituents, enhancing its reactivity in nucleophilic addition and condensation reactions. This bench-stable compound integrates readily into complex molecular architectures, serving as a key building block in synthetic organic chemistry and pharmaceutical intermediates.
2-Chloro-4-nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized aromatic systems. Its dual electron-withdrawing groups (nitro and chloro) enhance electrophilicity at the aldehyde carbon, facilitating nucleophilic addition and condensation reactions. The compound exhibits good bench stability and compatibility with common protecting group strategies, supporting its use in multi-step syntheses requiring selective 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: