CAS 71460-02-1
:4-Pentynoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methylester, (2S)-
Description:
4-Pentynoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester, with the CAS number 71460-02-1, is an organic compound characterized by its unique structure that includes a pentynoic acid moiety and a methyl ester functional group. This compound features a terminal alkyne, which contributes to its reactivity, particularly in coupling reactions and other organic transformations. The presence of the 1,1-dimethylethoxycarbonyl group indicates that it has protective characteristics, often used in synthetic organic chemistry to shield reactive amine functionalities. The (2S)-configuration suggests chirality, which can influence the compound's biological activity and interactions. Typically, compounds like this may be utilized in pharmaceutical applications, as intermediates in organic synthesis, or in the development of agrochemicals. Its solubility and stability can vary based on the solvent and environmental conditions, making it important to consider these factors in practical applications. Overall, this compound exemplifies the complexity and utility of organic molecules in chemical synthesis and research.
Formula:C11H17NO4
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Found 3 products.
(2S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-4-pentynoic acid methyl ester
CAS:Formula:C11H17NO4Purity:97%Color and Shape:SolidMolecular weight:227.2570Methyl (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate
CAS:Methyl (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoatePurity:97%Molecular weight:227.26g/mol


