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Structure of 1022159-15-4
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trans-tert-Butyl 4-aminocyclohexanecarboxylate delivers a stereochemically defined, bench-stable scaffold for asymmetric synthesis. The protected amine and cyclohexane ring enable efficient incorporation into bioactive molecules, while the tert-butyl ester facilitates selective deprotection under mild conditions. This compound serves as a key intermediate in medicinal chemistry campaigns targeting GPCR modulators and CNS therapeutics.
trans-tert-Butyl 4-aminocyclohexanecarboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to substituted cyclohexane scaffolds. The protected amine and ester functionalities offer orthogonal reactivity, facilitating sequential transformations. Its trans-configuration imparts defined stereochemistry, while the tert-butyl group ensures bench stability and ease of purification. Functions effectively in coupling reactions, reductive amination, and heterocycle formation.
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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: