2-(2,2,2-Trifluoroethoxy)pyrimidine-5-carboxylic acid

97%

Reagent Code: #241738
fingerprint
CAS Number 944905-08-2

science Other reagents with same CAS 944905-08-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.12 g/mol
Formula C₇H₅F₃N₂O₃
badge Registry Numbers
MDL Number MFCD10696903
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its structure supports binding to enzyme active sites, enhancing biological activity. The trifluoroethoxy group improves metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for better oral bioavailability and target selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to refine potency and pharmacokinetic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,040.00
inventory 250mg
10-20 days ฿34,080.00
2-(2,2,2-Trifluoroethoxy)pyrimidine-5-carboxylic acid
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its structure supports binding to enzyme active sites, enhancing biological activity. The trifluoroethoxy group improves metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for better oral bioavailability and target selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to refine

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its structure supports binding to enzyme active sites, enhancing biological activity. The trifluoroethoxy group improves metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for better oral bioavailability and target selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to refine potency and pharmacokinetic properties.

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...