(S)-N-(5-(3-Fluorobenzyl)-4H-1,2,4-triazol-3-yl)tetrahydrofuran-2-carboxamide

97%

Reagent Code: #237535
fingerprint
CAS Number 1645486-93-6

science Other reagents with same CAS 1645486-93-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.29 g/mol
Formula C₁₄H₁₅FN₄O₂
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) NS5A inhibitors. Its structural features enable strong binding to viral proteins, enhancing the potency of the drug candidate. It is also employed in medicinal chemistry research for optimizing pharmacokinetic properties in new drug entities targeting RNA viruses. The compound's chirality plays a critical role in biological activity, making the (S)-enantiomer preferred in active pharmaceutical ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿50,400.00
(S)-N-(5-(3-Fluorobenzyl)-4H-1,2,4-triazol-3-yl)tetrahydrofuran-2-carboxamide
No image available

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) NS5A inhibitors. Its structural features enable strong binding to viral proteins, enhancing the potency of the drug candidate. It is also employed in medicinal chemistry research for optimizing pharmacokinetic properties in new drug entities targeting RNA viruses. The compound's chirality plays a critical role in biological activity, making the (S)-enantiomer preferred in active pha

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) NS5A inhibitors. Its structural features enable strong binding to viral proteins, enhancing the potency of the drug candidate. It is also employed in medicinal chemistry research for optimizing pharmacokinetic properties in new drug entities targeting RNA viruses. The compound's chirality plays a critical role in biological activity, making the (S)-enantiomer preferred in active pharmaceutical ingredients.

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...