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Structure of 132076-27-8
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(R)-3-Oxo-cyclopentanecarboxylic acid methyl ester features a chiral cyclopentanone core with a strategically positioned ester group, enabling direct incorporation into asymmetric synthesis workflows. The carbonyl functionality supports enantioselective transformations, while the methyl ester enhances solubility and stability under standard bench conditions. This configuration facilitates efficient access to bioactive cyclopentane derivatives in medicinal chemistry and natural product synthesis.
(R)-3-Oxo-cyclopentanecarboxylic acid methyl ester serves as a valuable chiral building block in synthetic organic chemistry, enabling stereoselective synthesis of cyclopentane-containing pharmacophores. Its enantioselectively defined stereochemistry and ketone functionality facilitate diverse transformations, including nucleophilic additions, aldol reactions, and transition-metal-catalyzed couplings. The methyl ester group provides convenient handle for further derivatization or hydrolysis, while the compound exhibits good bench stability and ease of purification—making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: