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Structure of 912342-10-0
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(R)-Methyl 4-(1-aminoethyl)benzoate features a chiral α-amino ester scaffold with high stereochemical purity, enabling selective incorporation into peptide mimetics and bioactive small molecules. The pendant amine facilitates conjugation and derivatization under mild conditions, while the aromatic core enhances metabolic stability and solubility in organic media. This bench-stable reagent streamlines access to enantioselective building blocks for medicinal chemistry campaigns.
(R)-Methyl 4-(1-aminoethyl)benzoate serves as a chiral building block for medicinal chemistry, enabling efficient access to β-aryl-α-amino acid derivatives via standard peptide coupling and reduction protocols. Its bench-stable nature, combined with orthogonal functionality and high enantiomeric purity, facilitates straightforward incorporation into complex molecular architectures.
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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: