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Structure of 357405-75-5
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4-Bromo-2,5-difluorobenzaldehyde features a trifunctional aromatic core with bromine and two fluorine substituents positioned ortho and para to the aldehyde group. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a key building block for bioactive heterocycles and functional materials. The aldehyde functionality provides a handle for derivatization under mild conditions.
4-Bromo-2,5-difluorobenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling efficient Suzuki-Miyaura and Ullmann coupling reactions due to its orthogonal halogen reactivity. The aldehyde group facilitates direct functionalization via reductive amination or Grignard addition, while the difluoro substitution enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step synthesis of heterocyclic scaffolds and advanced pharmaceutical intermediates.
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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: