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Structure of 144001-42-3
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Methyl benzyl-DL-serinate offers a chiral, bench-stable amino acid derivative with enhanced solubility in organic solvents. This compound integrates a methyl ester and benzyl-protected serine scaffold, enabling direct use in peptide synthesis workflows without pre-activation. The DL-diastereomeric form provides access to diverse stereochemical configurations in modular coupling reactions.
Methyl benzyl-DL-serinate serves as a stable, bench-ready chiral building block for peptide and heterocyclic synthesis. Its dual functionality—ester and amino groups—enables straightforward derivatization via amidation, reduction, or coupling reactions. The benzyl protection group offers orthogonal stability under standard reaction conditions, facilitating selective transformations. This compound functions effectively in asymmetric synthesis workflows, providing access to diverse scaffolds with controlled stereochemistry.
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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: