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Structure of 99-61-6
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3-Nitrobenzaldehyde features a para-nitro group that enhances electrophilicity at the carbonyl center, enabling efficient nucleophilic addition reactions. This bench-stable aldehyde integrates readily into synthetic sequences requiring electron-deficient aromatic scaffolds.
3-Nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted heterocycles and pharmaceutical intermediates. Its dual functionality—aldehyde and meta-nitro group—permits selective transformations under standard conditions, including reductive amination, Mannich reactions, and coupling protocols. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H411
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Precautionary Statements : P264-P270-P273-P330-P391-P501
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Lot numbers can be found on the outside label of a product: