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Structure of 22647-95-6
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5-(4-Bromophenyl)pentanoic acid features a brominated aromatic ring linked via a flexible five-carbon chain to a carboxylic acid terminus. This structure enables integration into diverse synthetic scaffolds, particularly in medicinal chemistry and polymer functionalization. The para-bromine serves as a handle for further derivatization through cross-coupling reactions. The molecule exhibits good solubility in common organic solvents and maintains stability under standard bench conditions.
5-(4-Bromophenyl)pentanoic acid serves as a versatile building block for constructing bioactive scaffolds, enabling efficient Suzuki-Miyaura and Negishi coupling reactions due to its well-defined aryl bromide functionality. The aliphatic carboxylic acid group facilitates derivatization via esterification, amide formation, or decarboxylation protocols. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis in medicinal chemistry and materials science applications.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: