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Structure of 130309-46-5
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This cyclohexanecarboxylic acid derivative features a tert-butoxycarbonyl-protected amine group, offering enhanced stability and ease of handling in synthetic workflows. The bulky Boc moiety enables selective deprotection under mild acidic conditions, facilitating downstream functionalization. Ideal for peptide coupling and medicinal chemistry applications requiring controlled nitrogen protection.
4-((tert-Butoxycarbonyl)amino)cyclohexanecarboxylic acid serves as a versatile building block for the synthesis of bioactive cyclohexane-containing scaffolds. The tert-butoxycarbonyl (Boc) group provides excellent stability and orthogonal deprotection under mild acidic conditions, enabling efficient incorporation into peptide-like sequences and heterocyclic frameworks. Its carboxylic acid functionality facilitates direct coupling reactions, while the cyclohexane ring offers conformational rigidity useful in medicinal chemistry optimization. This compound enables robust, high-yielding transformations in standard synthetic 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: