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Structure of 37169-36-1
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(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoate is a chiral building block featuring a protected amino group and two adjacent hydroxyls on a phenyl ring. This configuration enables selective derivatization in peptide synthesis and glycosylation reactions. The tert-butoxycarbonyl (Boc) moiety provides stable protection under basic conditions, while the catechol functionality offers robust coordination for metal-catalyzed transformations.
(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoate serves as a key chiral building block for the synthesis of dopamine receptor ligands and catechol-containing pharmaceuticals. The protected amine enables orthogonal functionalization, while the ortho-dihydroxyphenyl group provides a versatile scaffold for metal-catalyzed coupling reactions and oxidation-sensitive transformations. Bench-stable and readily purified by chromatography, it functions efficiently in standard peptide and heterocyclic syntheses.
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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: