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Structure of 364385-64-8
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Methyl cis-4-(Boc-amino)cyclohexanecarboxylate features a stereodefined cyclohexane scaffold with a Boc-protected amine and ester functional group. This bench-stable, moisture-tolerant building block integrates readily into peptide synthesis and asymmetric catalysis workflows. The cis configuration ensures predictable conformational behavior in downstream transformations.
Methyl cis-4-(Boc-amino)cyclohexanecarboxylate serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to functionalized cyclohexane scaffolds. Its Boc-protected amine and ester groups offer orthogonal reactivity, facilitating selective transformations in multistep syntheses. The cis stereochemistry provides defined spatial control, enhancing predictability in downstream coupling and cyclization reactions. Bench-stable and readily purified by standard chromatography, it supports scalable applications in medicinal chemistry and process development.
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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: