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Structure of 4358-87-6
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Methyl DL-mandelate is a stable, bench-ready ester derivative of mandelic acid, offering enhanced solubility and reactivity in synthetic transformations. This chiral building block integrates readily into pharmaceutical intermediates and asymmetric synthesis workflows, providing a robust handle for downstream functionalization under standard conditions.
Methyl DL-mandelate serves as a stable, bench-ready chiral building block for asymmetric synthesis. It functions as a precursor in the construction of phenylalanine derivatives and other biologically relevant scaffolds, offering reliable enantioselective transformations under standard reaction conditions. The ester group enables straightforward derivatization, while the carboxylic acid functionality supports orthogonal functionalization—ideal for medicinal chemistry and process development workflows.
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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: