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Structure of 75877-66-6
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cis-Ethyl 4-hydroxycyclohexanecarboxylate features a hydroxyl group and ester functionality in close spatial proximity on a cyclohexane ring, enabling selective transformations. This stereochemically defined scaffold serves as a key intermediate in the synthesis of bioactive molecules and chiral building blocks. The cis configuration ensures predictable conformational behavior in downstream reactions.
cis-Ethyl 4-hydroxycyclohexanecarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations due to its defined equatorial hydroxyl and axial ester orientation. It functions as a key intermediate in the synthesis of bioactive molecules, particularly in medicinal chemistry and natural product derivatization, where controlled stereochemistry is critical. The compound exhibits excellent bench stability, facilitates straightforward functional group interconversions, and supports orthogonal protection strategies in complex molecule assembly.
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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: