Ethyl 1-(4-fluorophenyl)-1H-imidazole-4-carboxylate

97%

Reagent Code: #180592
fingerprint
CAS Number 114067-93-5

science Other reagents with same CAS 114067-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.23 g/mol
Formula C₁₂H₁₁FN₂O₂
thermostat Physical Properties
Boiling Point 358.3±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anti-inflammatory agents. Its structure supports activity against certain enzyme targets in pathogenic organisms. Commonly employed in medicinal chemistry for building imidazole-based drug candidates due to its favorable reactivity and ability to penetrate cell membranes. Also utilized in the preparation of fluorinated analogs to enhance metabolic stability and binding affinity in drug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,980.00
inventory 1g
10-20 days ฿68,750.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 1-(4-fluorophenyl)-1H-imidazole-4-carboxylate
No image available

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anti-inflammatory agents. Its structure supports activity against certain enzyme targets in pathogenic organisms. Commonly employed in medicinal chemistry for building imidazole-based drug candidates due to its favorable reactivity and ability to penetrate cell membranes. Also utilized in the preparation of fluorinated analogs to enhance metabolic stability and bindin

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anti-inflammatory agents. Its structure supports activity against certain enzyme targets in pathogenic organisms. Commonly employed in medicinal chemistry for building imidazole-based drug candidates due to its favorable reactivity and ability to penetrate cell membranes. Also utilized in the preparation of fluorinated analogs to enhance metabolic stability and binding affinity in drug design.

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...