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Structure of 885953-19-5
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3-Bromocyclopentane-1-carboxylic acid features a bromine substituent at the 3-position of a cyclopentane ring, flanked by a carboxylic acid group at the 1-position. This combination enables direct functionalization in synthetic transformations, particularly in nucleophilic substitution and cross-coupling reactions. The molecule exhibits enhanced reactivity due to the adjacent electron-withdrawing carboxylate, facilitating controlled derivatization under mild conditions.
3-Bromocyclopentane-1-carboxylic acid serves as a versatile building block for cyclopentane-based scaffolds, enabling direct functionalization at the C3 position. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports derivatization via amide formation or esterification. The molecule exhibits good bench stability and is readily purified by recrystallization, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: