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Structure of 34212-59-4
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This chiral succinate ester features a rigid, sterically defined cyclohexane core that enables precise stereochemical control in asymmetric synthesis. The isopropyl and methyl substituents enhance conformational stability and solubility, while the succinate linker provides a robust handle for derivatization. Ideal for catalytic applications requiring defined spatial orientation.
Bis((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl) succinate serves as a chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its rigid, well-defined stereochemistry. The molecule's bench-stable nature and predictable diastereoselectivity facilitate efficient enantioselective C–C bond formation. Its functional group tolerance supports broad utility in complex molecule assembly, particularly in the construction of cyclohexane-based scaffolds relevant to 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: