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Structure of 78537-14-1
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(R)-Methyl 2-amino-3-(tert-butoxy)propanoate hydrochloride features a chiral α-amino ester scaffold with a moisture-tolerant tert-butoxy group, enabling reliable use in asymmetric synthesis. This bench-stable derivative integrates seamlessly into peptide backbone elaborations and catalytic transformations, delivering high diastereoselectivity in key bond-forming steps.
(R)-Methyl 2-amino-3-(tert-butoxy)propanoate hydrochloride serves as a versatile chiral building block in peptide and heterocyclic synthesis. Its amine functionality enables straightforward derivatization, while the tert-butoxy group provides orthogonal protection for subsequent transformations. The hydrochloride salt enhances stability and solubility, facilitating handling and purification 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: