2-(Benzylamino)-2-oxoethyl 2-(furan-2-yl)quinoline-4-carboxylate

98%

Reagent Code: #131507
fingerprint
CAS Number 380173-16-0

science Other reagents with same CAS 380173-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.4 g/mol
Formula C₂₃H₁₈N₂O₄
thermostat Physical Properties
Boiling Point 666.4±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.277±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active quinoline derivatives, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its furan and benzylamino functional groups enable molecular diversification for structure-activity relationship studies. Commonly employed in medicinal chemistry for developing kinase inhibitors and fluorescent probes due to its conjugated aromatic system. Also applied in the preparation of organic semiconductors and optoelectronic materials because of its electron-transporting properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,690.00
inventory 250mg
10-20 days ฿45,370.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(Benzylamino)-2-oxoethyl 2-(furan-2-yl)quinoline-4-carboxylate
No image available

Used as a key intermediate in the synthesis of biologically active quinoline derivatives, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its furan and benzylamino functional groups enable molecular diversification for structure-activity relationship studies. Commonly employed in medicinal chemistry for developing kinase inhibitors and fluorescent probes due to its conjugated aromatic system. Also applied in the preparation of organic semiconductors and optoelectron

Used as a key intermediate in the synthesis of biologically active quinoline derivatives, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its furan and benzylamino functional groups enable molecular diversification for structure-activity relationship studies. Commonly employed in medicinal chemistry for developing kinase inhibitors and fluorescent probes due to its conjugated aromatic system. Also applied in the preparation of organic semiconductors and optoelectronic materials because of its electron-transporting 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...