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Structure of 74316-29-3
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Methyl trans-3-amino-cyclobutanecarboxylate hydrochloride features a rigid, conformationally constrained cyclobutane scaffold that stabilizes the amine orientation. This bench-stable derivative enables direct incorporation into peptide mimetics and bioactive scaffolds, offering enhanced metabolic resilience. The hydrochloride salt improves solubility and handling in aqueous reaction media.
Methyl trans-3-amino-cyclobutanecarboxylate hydrochloride serves as a conformationally constrained amino acid surrogate, enabling the synthesis of bioactive peptidomimetics and heterocyclic scaffolds. Its stable trans configuration and protected amine facilitate selective functionalization, while the ester group supports derivatization via standard amidation or reduction protocols. The hydrochloride salt enhances solubility and handling, making it suitable for bench-scale applications in medicinal chemistry and process development.
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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: