Diphenyl ((S)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)phosphoramidate

97%

Reagent Code: #168512
fingerprint
CAS Number 1860872-42-9

science Other reagents with same CAS 1860872-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 555.61 g/mol
Formula C₃₂H₃₄N₃O₄P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of antiviral drugs for the treatment of hepatitis C. Its chiral structure enables high selectivity in biological targeting, improving drug efficacy and reducing side effects. The phosphoramidate moiety is commonly employed in asymmetric synthesis routes to enhance cell permeability and metabolic stability, particularly in nucleotide analogs. Also utilized in the preparation of labeled compounds for metabolic studies and drug disposition assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Diphenyl ((S)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)phosphoramidate
No image available

Used as a key intermediate in the synthesis of antiviral drugs for the treatment of hepatitis C. Its chiral structure enables high selectivity in biological targeting, improving drug efficacy and reducing side effects. The phosphoramidate moiety is commonly employed in asymmetric synthesis routes to enhance cell permeability and metabolic stability, particularly in nucleotide analogs. Also utilized in the preparation of labeled compounds for metabolic studies and drug disposition assays.

Used as a key intermediate in the synthesis of antiviral drugs for the treatment of hepatitis C. Its chiral structure enables high selectivity in biological targeting, improving drug efficacy and reducing side effects. The phosphoramidate moiety is commonly employed in asymmetric synthesis routes to enhance cell permeability and metabolic stability, particularly in nucleotide analogs. Also utilized in the preparation of labeled compounds for metabolic studies and drug disposition assays.

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...