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Structure of 86123-95-7
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(R)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid features a chiral center with defined (R)-stereochemistry, enabling precise incorporation into peptide backbones. The tert-butoxycarbonyl group provides stable N-terminal protection, while the methoxy substituent enhances solubility and modulates electronic properties. This derivative supports efficient synthesis of bioactive peptides under standard bench conditions.
(R)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The protected amine and methoxy-functionalized side chain enable orthogonal reactivity in solid-phase and solution-phase synthesis. Bench-stable and readily purified by chromatography, it facilitates efficient access to complex scaffolds through standard coupling and cyclization protocols.
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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: