(3S,4S)-tert-Butyl 4-amino-3-hydroxypiperidine-1-carboxylate

98%

Reagent Code: #233335
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CAS Number 1161932-04-2

science Other reagents with same CAS 1161932-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD18072075
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its stereochemistry allows for selective interactions in biological systems, making it valuable in constructing complex drug molecules with high enantiomeric purity. Commonly employed in the preparation of HIV and HCV therapeutic agents due to its ability to mimic transition states in peptide bond hydrolysis. Also utilized in the synthesis of bioactive compounds requiring constrained piperidine scaffolds for enhanced metabolic stability and receptor binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,050.00
inventory 250mg
10-20 days ฿11,970.00
inventory 1g
10-20 days ฿32,290.00

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(3S,4S)-tert-Butyl 4-amino-3-hydroxypiperidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its stereochemistry allows for selective interactions in biological systems, making it valuable in constructing complex drug molecules with high enantiomeric purity. Commonly employed in the preparation of HIV and HCV therapeutic agents due to its ability to mimic transition states in peptide bond hydrolysis. Also utilized in the synthesis of bioactive compou

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its stereochemistry allows for selective interactions in biological systems, making it valuable in constructing complex drug molecules with high enantiomeric purity. Commonly employed in the preparation of HIV and HCV therapeutic agents due to its ability to mimic transition states in peptide bond hydrolysis. Also utilized in the synthesis of bioactive compounds requiring constrained piperidine scaffolds for enhanced metabolic stability and receptor binding affinity.

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