N-Boc-N-methoxy-3-aminopropionic acid is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, a methoxy group, and an amino acid backbone. This compound is typically used in organic synthesis, particularly in peptide chemistry, due to its ability to protect amino groups during reactions. The Boc group is a common protecting group that can be easily removed under acidic conditions, allowing for selective deprotection when needed. The methoxy group contributes to the compound's solubility and reactivity, making it a versatile intermediate in the synthesis of more complex molecules. Additionally, the presence of the carboxylic acid functional group allows for further derivatization, enabling the formation of various derivatives. N-Boc-N-methoxy-3-aminopropionic acid is generally stable under standard laboratory conditions but should be handled with care, as with all chemical substances, to avoid potential hazards. Its applications in medicinal chemistry and biochemistry highlight its importance in the development of pharmaceutical compounds.

N-Boc-N-methoxy-3-aminopropionic acid

172299-81-9: 3-(Tert-butoxycarbonyl(methoxy)amino)propanoic acid

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CAS 172299-81-9: N-Boc-N-methoxy-3-aminopropionic acid

3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid

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3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid

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N-Boc-N-methoxy-3-aminopropionic acid

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