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Structure of 5274-71-5
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2-Bromo-4-nitrobenzaldehyde features a bromine atom at the ortho position and a nitro group at the para position relative to the aldehyde, creating a highly electron-deficient aromatic ring. This combination enables efficient coupling in cross-coupling reactions and facilitates functionalization in synthetic pathways requiring strong electrophilic character.
2-Bromo-4-nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization via palladium-catalyzed cross-coupling reactions. The aldehyde group facilitates nucleophilic additions and condensation reactions, while the bromo and nitro substituents provide orthogonal reactivity for sequential transformations. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for constructing complex heterocycles and pharmaceutical intermediates.
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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: