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Structure of 127425-80-3
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This boronate-bearing compound features a bromo-fluoro-substituted phenyl ring linked to a propionic acid handle, enabling direct integration into Suzuki-Miyaura coupling reactions. The electron-deficient aryl moiety enhances reactivity while maintaining bench-stable handling under standard conditions.
3-(4-Bromo-3-fluorophenyl)propionic acid serves as a valuable building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and pharmaceutical development. Its well-defined aryl halogen substituents enable robust cross-coupling reactions, including Suzuki and Stille transformations. The carboxylic acid functionality facilitates direct derivatization or incorporation into peptide-like scaffolds, while the molecule exhibits good bench stability and ease of purification.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: