2-Deoxy-2,2-difluoro-D-erythro-pentonic acid γ-Lactone 3,5-dibenzoate

98%

Reagent Code: #64197
fingerprint
CAS Number 122111-01-7

science Other reagents with same CAS 122111-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.31 g/mol
Formula C₁₉H₁₄F₂O₆
badge Registry Numbers
MDL Number MFCD08458308
thermostat Physical Properties
Melting Point 117-119 °C(lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a key intermediate in the production of gemcitabine, a widely used chemotherapy agent. The difluoro substitution enhances the metabolic stability and biological activity of the resulting nucleoside analogs, making it valuable in medicinal chemistry. Additionally, its dibenzoate groups provide protection during synthetic processes, ensuring precise modifications to the molecule. This chemical plays a significant role in advancing pharmaceutical research, particularly in the design of targeted therapies for treating various diseases.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 121-125
Purity (HPLC) 98-100%
Specific Rotation (20°C, 1% CH3CN) 69-73
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿1,100.00
inventory 100g
10-20 days ฿4,110.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Deoxy-2,2-difluoro-D-erythro-pentonic acid γ-Lactone 3,5-dibenzoate
No image available

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a key intermediate in the production of gemcitabine, a widely used chemotherapy agent. The difluoro substitution enhances the metabolic stability and biological activity of the resulting nucleoside analogs, making it valuable in medicinal chemistry. Additionally, its dibenzoate groups provide protection during synthetic proce

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a key intermediate in the production of gemcitabine, a widely used chemotherapy agent. The difluoro substitution enhances the metabolic stability and biological activity of the resulting nucleoside analogs, making it valuable in medicinal chemistry. Additionally, its dibenzoate groups provide protection during synthetic processes, ensuring precise modifications to the molecule. This chemical plays a significant role in advancing pharmaceutical research, particularly in the design of targeted therapies for treating various diseases.

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...