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Structure of 876-05-1
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This chiral cyclopentane-1,3-dicarboxylic acid features a rigid, cis-configured scaffold ideal for probing stereochemical effects in medicinal chemistry. The proximal carboxylate groups enable straightforward derivatization and coordination in metal-ligand systems. Bench-stable and moisture-tolerant, it integrates seamlessly into synthetic routes requiring defined spatial orientation.
(1R,3S)-Cyclopentane-1,3-dicarboxylic acid serves as a valuable chiral building block in the synthesis of bioactive molecules and natural product analogs. Its defined stereochemistry enables predictable stereoselective transformations, while the dicarboxylic acid functionality offers versatile handles for derivatization, including esterification, amide formation, and metal coordination. The compound exhibits excellent bench stability and facilitates efficient purification via recrystallization or chromatography, making it well-suited for use in medicinal chemistry campaigns and catalyst 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-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: