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Structure of 17288-15-2
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Ethyl 2-amino-2-methylpropanoate hydrochloride features a sterically hindered α-amino ester core with enhanced solubility in polar solvents. This bench-stable derivative enables direct incorporation into peptide couplings and amine-functionalized intermediates without requiring protection. The protonated amine facilitates salt formation, improving handling and storage stability in synthetic workflows.
Ethyl 2-amino-2-methylpropanoate hydrochloride serves as a versatile building block in peptide and heterocyclic synthesis, offering a readily accessible tertiary amine with orthogonal reactivity. Its stability under standard conditions facilitates straightforward handling and purification, while the protected amine group enables efficient coupling reactions and incorporation into β-amino acid scaffolds. Functions effectively in Mannich-type cyclizations and as a precursor to bioactive amine-containing motifs.
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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: