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Structure of 6833-47-2
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trans-(1r,4r)-4-Ethylcyclohexane-1-carboxylic acid features a rigid, sterically defined cyclohexane core with equatorially oriented substituents, delivering predictable conformational behavior. The carboxylic acid group enables direct derivatization, while the ethyl moiety enhances lipophilicity and metabolic stability. This stereochemically pure scaffold supports applications in asymmetric synthesis and medicinal chemistry.
trans-(1r,4r)-4-Ethylcyclohexane-1-carboxylic acid serves as a stereochemically defined building block for cyclohexane-based scaffolds in medicinal chemistry and natural product synthesis. Its stable trans-configuration and carboxylic acid functionality enable straightforward derivatization, including amide formation and esterification, while maintaining predictable conformational rigidity. The molecule exhibits excellent bench stability and facilitates efficient purification via recrystallization or chromatography.
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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: