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Structure of 71830-06-3
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(S)-3-Oxocyclopentanecarboxylic acid features a chiral cyclopentane core bearing a ketone and carboxylic acid at adjacent positions, enabling selective transformations in asymmetric synthesis. This configuration supports stereoselective functionalization in medicinal chemistry and natural product derivatization.
(S)-3-Oxocyclopentanecarboxylic acid serves as a valuable chiral building block in synthetic organic chemistry, enabling stereoselective synthesis of bioactive molecules. Its cyclopentanone core facilitates diverse transformations, including enolate alkylation and nucleophilic addition reactions. The carboxylic acid functionality supports direct derivatization or coupling protocols, while the stereochemical integrity ensures predictable reactivity in asymmetric synthesis workflows. Bench-stable and readily purified, it functions effectively in medicinal chemistry and natural product synthesis.
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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: