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Structure of 1370025-54-9
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2-Bromo-6-fluoro-4-methylbenzaldehyde features a trifunctional aromatic core with bromo, fluoro, and methyl groups positioned ortho to the aldehyde. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in pharmaceutical synthesis. The aldehyde functionality offers high reactivity for nucleophilic additions and condensations under mild conditions.
2-Bromo-6-fluoro-4-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted aromatic scaffolds. Its orthogonal halogenation pattern facilitates palladium-catalyzed cross-coupling reactions, while the aldehyde group supports nucleophilic additions and condensation processes. The compound exhibits excellent bench stability and is compatible with standard purification protocols, making it well-suited for multi-step synthetic sequences requiring functional group tolerance and predictable reactivity.
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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
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Precautionary Statements : P261-P280-P304+P340-P405
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Lot numbers can be found on the outside label of a product: