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Structure of 1639298-89-7
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4-Chloro-2-fluoro-5-nitrobenzaldehyde features a trifunctional aromatic core integrating electron-withdrawing halogens and a nitro group, enabling efficient coupling in cross-coupling and multistep synthesis. This bench-stable aldehyde integrates readily into pharmaceutical intermediates and functional materials, offering high reactivity under standard conditions.
4-Chloro-2-fluoro-5-nitrobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via electrophilic aromatic substitution and coupling reactions. Its ortho-fluoro and para-chloro directing groups facilitate regioselective functionalization, while the aldehyde and nitro functionalities offer complementary handles for downstream transformations. Bench-stable and compatible with standard reaction conditions, it functions effectively in multi-step syntheses requiring precise positional control.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314-H317-H318
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Precautionary Statements : P260-P264-P270-P272-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: