(R)-Methyl 2-amino-2-(2,4-difluorophenyl)acetate hydrochloride

97%

Reagent Code: #113519
fingerprint
CAS Number 1958125-88-6

science Other reagents with same CAS 1958125-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.63 g/mol
Formula C₉H₁₀ClF₂NO₂
badge Registry Numbers
MDL Number MFCD22638196
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of antifungal agents, particularly those targeting fungal infections caused by pathogens like Candida and Aspergillus species. The compound's structure, featuring a difluorophenyl group, enhances its binding affinity to specific biological targets, making it valuable in drug design. Additionally, it is utilized in research settings to study enzyme inhibition and receptor interactions, contributing to the discovery of new therapeutic agents. Its chiral nature also makes it significant in the production of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,654.00
inventory 100mg
10-20 days ฿6,327.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-Methyl 2-amino-2-(2,4-difluorophenyl)acetate hydrochloride
No image available
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of antifungal agents, particularly those targeting fungal infections caused by pathogens like Candida and Aspergillus species. The compound's structure, featuring a difluorophenyl group, enhances its binding affinity to specific biological targets, making it valuable in drug design. Additionally, it is utilized in research settings to study enzyme inhibition and receptor interactions, contributing to the discovery of new therapeutic agents. Its chiral nature also makes it significant in the production of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects.
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...