2-Tert-Butoxycarbonylamino-pent-4-ynoic acid methyl ester, with the CAS number 173306-82-6, is a chemical compound characterized by its functional groups and structural features. It contains a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during reactions. The presence of a pent-4-ynoic acid moiety indicates that it has a five-carbon chain with a terminal alkyne, contributing to its reactivity and potential applications in synthesis. The methyl ester functionality suggests that it can undergo hydrolysis to yield the corresponding carboxylic acid, making it versatile in various chemical reactions. This compound is typically utilized in peptide synthesis and other organic transformations due to its ability to facilitate the introduction of amino acids or other functional groups. Its stability and reactivity can be influenced by the steric hindrance provided by the tert-butyl group, making it an interesting candidate for further chemical exploration in medicinal chemistry and related fields.

2-TERT-BUTOXYCARBONYLAMINO-PENT-4-YNOIC ACID METHYL ESTER

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CAS 173306-82-6: 2-TERT-BUTOXYCARBONYLAMINO-PENT-4-YNOIC ACID METHYL ESTER

4-Pentynoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester

Ref: IN-DA001YRN

Methyl 2-{[(tert-butoxy)carbonyl]amino}pent-4-ynoate

Ref: 3D-YGA30682

N-Boc-Propargylglycine methyl ester

Ref: 10-F046641