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Structure of 149947-15-9
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3-Bromo-2-fluorobenzaldehyde features a bromine atom at the meta position and a fluorine substituent at the ortho position relative to the aldehyde group, creating a uniquely electron-deficient aromatic ring. This configuration enhances reactivity in transition-metal-catalyzed coupling processes. The compound exhibits bench-stable handling characteristics and integrates readily into complex molecular architectures.
3-Bromo-2-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The ortho-fluoro substituent enhances metabolic stability while the aldehyde group facilitates imine formation and reductive amination. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses of heterocyclic scaffolds and functionalized aryl derivatives.
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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: