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Structure of 7686-77-3
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Cyclopent-3-enecarboxylic acid features a conjugated enone system that enhances reactivity in Diels-Alder and Michael addition reactions. The carboxylic acid group provides a handle for derivatization, while the rigid cyclopentene scaffold imparts structural definition. This compound serves as a valuable building block in synthetic organic chemistry and natural product synthesis.
Cyclopent-3-enecarboxylic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclopentane derivatives through functional group transformations. Its conjugated enoic acid structure facilitates Diels-Alder reactions and metal-catalyzed couplings, while the carboxylic acid group supports direct derivatization or activation for peptide coupling and esterification. Bench-stable and amenable to purification by recrystallization, it functions reliably in multi-step syntheses targeting bioactive heterocycles and natural product analogs.
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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 : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: