CAS 203662-91-3: ethyl {4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}acetate

Description: Ethyl {4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}acetate, identified by its CAS number 203662-91-3, is a chemical compound that features a piperidine ring substituted with an ethyl acetate group and a tert-butoxycarbonyl (Boc) amino group. This compound is characterized by its moderate polarity due to the presence of both hydrophobic (tert-butoxy) and hydrophilic (acetate) functional groups. The piperidine moiety contributes to its potential as a building block in organic synthesis, particularly in the development of pharmaceuticals. The Boc group serves as a protective group for the amine, allowing for selective reactions without affecting the amine functionality. Ethyl {4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}acetate is typically a solid or liquid at room temperature, depending on its purity and specific formulation. Its stability and reactivity can be influenced by environmental factors such as temperature and pH. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its structural features and potential applications.

Formula: C₁₄H₂₆N₂O₄

InChI: InChI=1/C14H26N2O4/c1-5-19-12(17)10-16-8-6-11(7-9-16)15-13(18)20-14(2,3)4/h11H,5-10H2,1-4H3,(H,15,18)

Synonyms:

• Ethyl {4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}acetate

Ethyl 2-(4-{[(tert-butoxy)carbonyl]amino}piperidin-1-yl)acetate

CAS: 203662-91-3

• Molecular weight: 286.36724g/mol

Ethyl 2-(4-{[(tert-butoxy)carbonyl]amino}piperidin-1-yl)acetate

CAS: 203662-91-3

Versatile small molecule scaffold

• Formula: C₁₄H₂₆N₂O₄
• Purity: Min. 95%
• Molecular weight: 286.37 g/mol

(4-Boc-Amino-piperidin-1-yl)acetic acid ethylester

CAS: 203662-91-3

• Purity: 98.0%
• Color and Shape: Solid
• Molecular weight: 286.37200927734375