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Structure of 90940-54-8
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(R)-Ethyl 2-amino-4-phenylbutanoate hydrochloride features a chiral α-amino acid scaffold with a phenyl-substituted aliphatic chain, delivering high enantiomeric purity for asymmetric synthesis. This bench-stable, moisture-tolerant derivative serves as a key building block in peptide analogs and bioactive molecule construction.
(R)-Ethyl 2-amino-4-phenylbutanoate hydrochloride serves as a key chiral building block for the synthesis of biologically relevant heterocycles and amino acid derivatives. Its well-defined stereochemistry enables reliable asymmetric synthesis, while the protected amine and ester functionalities offer orthogonal reactivity for sequential transformations. The hydrochloride salt enhances bench stability and simplifies purification, making it suitable for scalable peptide and medicinal chemistry applications.
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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: