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Structure of 6628-86-0
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5-Chloro-2-nitrobenzaldehyde features a chlorine substituent at the meta position and a nitro group at the ortho position relative to the aldehyde, creating a strongly electron-deficient aromatic ring. This configuration enhances reactivity in nucleophilic addition and condensation reactions. The compound exhibits bench-stable handling characteristics and integrates readily into complex synthetic sequences requiring polarized carbonyl functionality.
5-Chloro-2-nitrobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via condensation and cyclization reactions. Its electron-deficient aromatic core enhances reactivity in nucleophilic aromatic substitution, while the aldehyde and nitro groups provide orthogonal functional handles for sequential transformations. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of complex scaffolds.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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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 : H290-H315-H317-H318-H335-H400
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Precautionary Statements : P234-P261-P261-P273-P280-P280-P302+P352-P302+P352
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Lot numbers can be found on the outside label of a product: