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

≥95%

Reagent Code: #230459
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CAS Number 443955-98-4

science Other reagents with same CAS 443955-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD18425632
thermostat Physical Properties
Boiling Point 326.1±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and central nervous system drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for constructing enantiomerically pure active pharmaceutical ingredients. Commonly employed in the preparation of protease inhibitors and receptor modulators due to the presence of functionalized piperidine scaffold. The protected amine and hydroxyl groups allow for stepwise derivatization in multi-step synthetic routes, enhancing flexibility in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,880.00
inventory 250mg
10-20 days ฿5,190.00
inventory 1g
10-20 days ฿14,720.00
inventory 10g
10-20 days ฿89,600.00
inventory 5g
10-20 days ฿48,000.00

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(3R,4R)-rel-tert-Butyl 4-amino-3-hydroxypiperidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and central nervous system drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for constructing enantiomerically pure active pharmaceutical ingredients. Commonly employed in the preparation of protease inhibitors and receptor modulators due to the presence of functionalized piperidine scaffold. The protected amine and hydroxyl groups allow
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and central nervous system drugs. Its stereochemistry enables selective interactions in biological systems, making it valuable for constructing enantiomerically pure active pharmaceutical ingredients. Commonly employed in the preparation of protease inhibitors and receptor modulators due to the presence of functionalized piperidine scaffold. The protected amine and hydroxyl groups allow for stepwise derivatization in multi-step synthetic routes, enhancing flexibility in drug design.
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