(2R,3S)-tert-Butyl 3-hydroxy-2-methylazetidine-1-carboxylate

98%

Reagent Code: #232292
fingerprint
CAS Number 1638744-13-4

science Other reagents with same CAS 1638744-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD28501319
thermostat Physical Properties
Boiling Point 263.0±33.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its strained azetidine ring and defined stereochemistry make it valuable for constructing conformationally restricted scaffolds in drug design. Commonly employed in medicinal chemistry to improve metabolic stability and binding selectivity. Also utilized in the preparation of enzyme inhibitors where the hydroxy and carbamate functionalities allow for further chemical modifications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,460.00
inventory 250mg
10-20 days ฿7,150.00
inventory 500mg
10-20 days ฿10,000.00
inventory 1g
10-20 days ฿14,260.00
inventory 5g
10-20 days ฿46,800.00
(2R,3S)-tert-Butyl 3-hydroxy-2-methylazetidine-1-carboxylate
No image available

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its strained azetidine ring and defined stereochemistry make it valuable for constructing conformationally restricted scaffolds in drug design. Commonly employed in medicinal chemistry to improve metabolic stability and binding selectivity. Also utilized in the preparation of enzyme inhibitors where the hydroxy and carbamate functionalities all

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its strained azetidine ring and defined stereochemistry make it valuable for constructing conformationally restricted scaffolds in drug design. Commonly employed in medicinal chemistry to improve metabolic stability and binding selectivity. Also utilized in the preparation of enzyme inhibitors where the hydroxy and carbamate functionalities allow for further chemical modifications.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...