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Structure of 53292-89-0
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trans-4-(Boc-Amino)cyclohexanecarboxylic acid features a rigid, conformationally stable cyclohexane scaffold with a Boc-protected amino group positioned trans to the carboxylic acid. This stereochemical configuration enhances solubility and stability during peptide coupling workflows. The protected amine facilitates direct incorporation into peptidic sequences without side-reaction interference.
trans-4-(Boc-Amino)cyclohexanecarboxylic acid serves as a versatile chiral building block for the synthesis of bioactive molecules and heterocyclic scaffolds. The Boc-protected amine exhibits excellent bench stability and compatibility with standard coupling conditions, enabling straightforward incorporation into peptide-like architectures. Its rigid trans-cyclohexane framework provides defined stereochemistry and conformational restraint, facilitating predictable reactivity in functional group interconversions and ring-forming processes.
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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: