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Structure of 1391439-19-2
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(S)-Methyl 3-(1-aminoethyl)benzoate hydrochloride features a chiral α-amino acid ester core with enhanced solubility and stability under standard conditions. This bench-stable derivative integrates seamlessly into peptide coupling workflows, enabling efficient access to non-natural amino acid building blocks for medicinal chemistry and synthetic biology applications.
(S)-Methyl 3-(1-aminoethyl)benzoate hydrochloride serves as a chiral building block for asymmetric synthesis, enabling direct access to biologically relevant (S)-configured arylalanine derivatives. The protected amine and ester functionalities offer orthogonal reactivity, facilitating downstream modifications in peptide and medicinal chemistry workflows. Bench-stable and readily purified by standard methods, it functions reliably in coupling reactions and reductive amination protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: