N-Cbz-3-piperidineacetic acid methyl ester, with the CAS number 86827-08-9, is a chemical compound that features a piperidine ring, which is a six-membered nitrogen-containing heterocycle. This compound is characterized by the presence of a carbobenzyloxy (Cbz) protecting group, which is commonly used in organic synthesis to protect amines. The methyl ester functional group indicates that the carboxylic acid moiety is esterified with methanol, enhancing its solubility and reactivity in various chemical reactions. The presence of the piperidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. This compound is typically utilized in the synthesis of more complex molecules, particularly in the development of pharmaceuticals. Its properties, such as solubility, stability, and reactivity, can vary based on the specific conditions under which it is handled, including temperature and solvent choice. Overall, N-Cbz-3-piperidineacetic acid methyl ester serves as a versatile intermediate in organic synthesis and drug development.

N-Cbz-3-piperidineacetic acid methyl ester

86827-08-9: Methyl 3-(N-Cbz-piperidinoxy)acetate, Benzyl 3-(2-Methoxy-2-Oxoethyl)Piperidine-1-Carboxylate

_x005F_x000D_Methyl N-Cbz-3-piperidylacetate

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CAS 86827-08-9: N-Cbz-3-piperidineacetic acid methyl ester

_x005F_x000D_Methyl N-Cbz-3-piperidylacetate

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Methyln-cbz-3-piperidineacetate

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Methyl N-Cbz-3-piperidylacetate

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