(2R,4S)-tert-Butyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate

95%

Reagent Code: #231477
fingerprint
CAS Number 77450-03-4

science Other reagents with same CAS 77450-03-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.27 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD11617835
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its chiral structure with multiple functional groups allows for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in medicinal chemistry for constructing complex nitrogen-containing heterocycles with biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,630.00
inventory 250mg
10-20 days ฿18,060.00
inventory 1g
10-20 days ฿48,730.00
(2R,4S)-tert-Butyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its chiral structure with multiple functional groups allows for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in medicinal chemistry for constructing complex nitrogen-containing heterocycles with biolog

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its chiral structure with multiple functional groups allows for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in medicinal chemistry for constructing complex nitrogen-containing heterocycles with biological activity.

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...