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Structure of 284047-98-9
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3-Nitro-5-(trifluoromethyl)benzaldehyde features a strongly electron-deficient aromatic ring bearing both nitro and trifluoromethyl groups, enabling efficient coupling in cross-coupling reactions. The aldehyde functionality provides a direct handle for nucleophilic addition or condensation chemistry, offering high reactivity under standard conditions. This compound serves as a valuable building block in pharmaceutical and agrochemical synthesis.
3-Nitro-5-(trifluoromethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted heterocycles and functionalized aromatic systems. Its electron-deficient aromatic core enhances reactivity in nucleophilic addition and condensation reactions, while the trifluoromethyl group imparts metabolic stability and modulates lipophilicity. Bench-stable and compatible with standard purification protocols, it facilitates scalable synthesis of complex scaffolds.
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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: