1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose

98%

Reagent Code: #103814
fingerprint
CAS Number 171721-00-9

science Other reagents with same CAS 171721-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.44 g/mol
Formula C₂₆H₂₁FO₇
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as a key intermediate in the modification of sugar moieties, enabling the creation of compounds with enhanced biological activity and specificity. Its fluorinated structure is particularly valuable in medicinal chemistry, as it can improve the metabolic stability and binding affinity of the resulting molecules. Researchers utilize it to explore new therapeutic agents, especially in the field of antiviral research, where modified nucleosides play a significant role in inhibiting viral replication. Additionally, its benzoyl groups provide protection during synthetic processes, ensuring precise and controlled reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless Solid or White to Off-White Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,073.00
inventory 10g
10-20 days ฿14,391.00
inventory 1g
10-20 days ฿2,106.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose
No image available

This chemical is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as a key intermediate in the modification of sugar moieties, enabling the creation of compounds with enhanced biological activity and specificity. Its fluorinated structure is particularly valuable in medicinal chemistry, as it can improve the metabolic stability and binding affinity of the resulting molecules. Researchers utilize it to explore new ther

This chemical is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as a key intermediate in the modification of sugar moieties, enabling the creation of compounds with enhanced biological activity and specificity. Its fluorinated structure is particularly valuable in medicinal chemistry, as it can improve the metabolic stability and binding affinity of the resulting molecules. Researchers utilize it to explore new therapeutic agents, especially in the field of antiviral research, where modified nucleosides play a significant role in inhibiting viral replication. Additionally, its benzoyl groups provide protection during synthetic processes, ensuring precise and controlled reactions.

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...