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Structure of 1703-61-3
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4-Oxocyclopentane-1,2-dicarboxylic acid features a rigid cyclopentane core with two adjacent carboxylic acid groups and a strategically positioned ketone at the C4 position. This configuration enables selective metal chelation and serves as a key scaffold in bioactive molecule design. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions.
4-Oxocyclopentane-1,2-dicarboxylic acid serves as a versatile building block in synthetic organic chemistry, enabling the construction of substituted cyclopentane scaffolds prevalent in bioactive molecules. Its orthogonal functionality—combining a ketone and two carboxylic acid groups—facilitates selective derivatization, including esterification, amide formation, and reductive transformations. The compound exhibits good bench stability and is compatible with standard purification techniques, making it suitable for use in medicinal chemistry campaigns and process development workflows.
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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: