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Structure of 3618-04-0
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trans-Ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate is a stereochemically defined cyclohexane derivative featuring a hydroxyl group in axial orientation and an ester functionality at the opposite ring position. This configuration imparts enhanced conformational rigidity and predictable reactivity in asymmetric synthesis. The compound serves as a key chiral building block for natural product analogs and pharmaceutical intermediates.
trans-Ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate serves as a stereochemically defined building block for cyclohexane-based scaffolds, enabling access to functionalized intermediates in natural product and medicinal chemistry synthesis. Its stable trans-diastereomer configuration facilitates predictable regioselective transformations, while the pendant hydroxyl and ester groups offer orthogonal handles for further derivatization. The compound exhibits excellent bench stability and is readily purified by standard chromatographic methods, supporting its use in scalable synthetic 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: