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Structure of 5326-50-1
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Ethyl 2-(1-hydroxycyclohexyl)acetate features a cyclohexanol-derived chiral center paired with an ester-functionalized side chain, enabling direct incorporation into asymmetric synthesis. The pendant hydroxyl group offers a handle for derivatization, while the ester moiety supports selective transformations under mild conditions. This structure combines stability with reactivity, making it suitable for building complex molecular architectures in medicinal chemistry and natural product synthesis.
Ethyl 2-(1-hydroxycyclohexyl)acetate serves as a versatile building block for cyclohexyl-containing scaffolds, enabling efficient access to functionalized terpenoid-like architectures. The pendant hydroxyl group facilitates selective derivatization, while the ester functionality supports transformations such as reduction, hydrolysis, or coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthesis in medicinal chemistry 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: