(R)-tert-Butyl 3-((6-(cyclopropylamino)pyrimidin-4-yl)oxy)pyrrolidine-1-carboxylate

95%

Reagent Code: #228686
fingerprint
CAS Number 1417789-30-0

science Other reagents with same CAS 1417789-30-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.39 g/mol
Formula C₁₆H₂₄N₄O₃
badge Registry Numbers
MDL Number MFCD22631758
thermostat Physical Properties
Boiling Point 484.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.273±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in creating protease or polymerase inhibitors. The compound's chiral center and functional groups support high specificity and potency in drug design, especially in orally available therapeutics. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties such as metabolic stability and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,960.00
inventory 100mg
10-20 days ฿11,840.00
(R)-tert-Butyl 3-((6-(cyclopropylamino)pyrimidin-4-yl)oxy)pyrrolidine-1-carboxylate
No image available

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in creating protease or polymerase inhibitors. The compound's chiral center and functional groups support high specificity and potency in drug design, especially in orally available therapeutics. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties such as m

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in creating protease or polymerase inhibitors. The compound's chiral center and functional groups support high specificity and potency in drug design, especially in orally available therapeutics. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties such as metabolic stability and bioavailability.

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...