(1R)-1-(oxetan-3-yl)ethan-1-amine

97%

Reagent Code: #228719
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CAS Number 1426426-79-0

science Other reagents with same CAS 1426426-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD27938781
thermostat Physical Properties
Boiling Point 143.5±13.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.998±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of protease inhibitors and antiviral agents. Its rigid oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system (CNS) active compounds due to its favorable polarity and ability to cross the blood-brain barrier. Also utilized in the design of novel antibiotics where stereochemistry and ring strain contribute to target selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,520.00
inventory 500mg
10-20 days ฿38,730.00
(1R)-1-(oxetan-3-yl)ethan-1-amine
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Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of protease inhibitors and antiviral agents. Its rigid oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system (CNS) active compounds due to its favorable polarity and ability to cross the blood-brain barrier. Also utilized in the design of novel antibiotics where stereochemistry

Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of protease inhibitors and antiviral agents. Its rigid oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system (CNS) active compounds due to its favorable polarity and ability to cross the blood-brain barrier. Also utilized in the design of novel antibiotics where stereochemistry and ring strain contribute to target selectivity.

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