(R)-tert-Butyl (2-oxooxetan-3-yl)carbamate

95%

Reagent Code: #217147
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CAS Number 126330-77-6

science Other reagents with same CAS 126330-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.2 g/mol
Formula C₈H₁₃NO₄
badge Registry Numbers
MDL Number MFCD11519129
thermostat Physical Properties
Boiling Point 318.989 ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.185 g/cm3
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of nucleoside analogs. Its chiral oxetane structure enhances metabolic stability and bioavailability in pharmaceutical compounds. Commonly employed in medicinal chemistry for modifying sugar moieties to improve drug resistance and binding affinity to viral polymerases. Also utilized in the development of protease inhibitors due to its ability to mimic peptide transition states.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿720.00
500mg
10-20 days ฿1,590.00
1g
10-20 days ฿2,720.00
5g
10-20 days ฿12,000.00
10g
10-20 days ฿22,400.00
(R)-tert-Butyl (2-oxooxetan-3-yl)carbamate
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Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of nucleoside analogs. Its chiral oxetane structure enhances metabolic stability and bioavailability in pharmaceutical compounds. Commonly employed in medicinal chemistry for modifying sugar moieties to improve drug resistance and binding affinity to viral polymerases. Also utilized in the development of protease inhibitors due to its ability to mimic peptide transition states.

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of nucleoside analogs. Its chiral oxetane structure enhances metabolic stability and bioavailability in pharmaceutical compounds. Commonly employed in medicinal chemistry for modifying sugar moieties to improve drug resistance and binding affinity to viral polymerases. Also utilized in the development of protease inhibitors due to its ability to mimic peptide transition states.

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