Benzyl (3S,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate
95%
Reagent
Code: #82889
CAS Number
1549812-60-3
blur_circular Chemical Specifications
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Molecular Information
Weight
350.42 g/mol
Formula
C₁₈H₂₆N₂O₅
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Registry Numbers
MDL Number
MFCD31656832
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Physical Properties
Boiling Point
512.9±50.0 °C(Predicted)
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Storage & Handling
Density
1.22±0.1 g/cm3(Predicted)
Storage
Room temperature, sealed, dry
description Product Description
This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors and other therapeutic molecules targeting various diseases. Its structure, featuring both a Boc-protected amino group and a hydroxyl group, makes it a valuable intermediate in organic synthesis, enabling the construction of intricate molecular frameworks. It is often employed in peptide chemistry and medicinal chemistry research, where precise control over stereochemistry and functional group manipulation is crucial. Additionally, it serves as a building block in the preparation of biologically active compounds, contributing to advancements in drug discovery and development.
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Benzyl (3S,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors and other therapeutic molecules targeting various diseases. Its structure, featuring both a Boc-protected amino group and a hydroxyl group, makes it a valuable intermediate in organic synthesis, enabling the construction of intricate molecular frameworks. It is often employed in peptide chemistry and medicinal chemistry research, where precise control over stereochemistry and functional group manipulation is crucial. Additionally, it serves as a building block in the preparation of biologically active compounds, contributing to advancements in drug discovery and development.
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