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Structure of 21963-41-7
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This chiral cyclohexane derivative features a rigid, trans-configured dicarboxylic acid scaffold ideal for asymmetric synthesis and molecular recognition studies. The stereochemically defined carboxyl groups enable precise spatial control in ligand design and catalytic systems.
(1S,2S)-Cyclohexane-1,2-dicarboxylic acid serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in medicinal chemistry and natural product synthesis. Its rigid cyclohexane framework provides defined stereochemistry, while the dicarboxylic acid functionality facilitates derivatization via esterification, amide formation, or salt formation. The compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable applications in API intermediate development and catalyst design.
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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: