Ethyl 4-hydroxy-7-methoxyquinoline-3-carboxylate

98%

Reagent Code: #184243
fingerprint
CAS Number 63463-15-0

science Other reagents with same CAS 63463-15-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.25 g/mol
Formula C₁₃H₁₃NO₄
badge Registry Numbers
MDL Number MFCD00085986
thermostat Physical Properties
Boiling Point 373.2±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibiotics and antiviral agents. Its structure supports the formation of bioactive molecules with potent antimicrobial properties. Commonly employed in medicinal chemistry for constructing fused quinoline systems that exhibit enhanced binding to DNA gyrase and topoisomerase enzymes. Also utilized in research settings to design novel heterocyclic compounds with potential anticancer and anti-inflammatory activities.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿660.00
inventory 25g
10-20 days ฿14,530.00
inventory 5g
10-20 days ฿3,140.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 4-hydroxy-7-methoxyquinoline-3-carboxylate
No image available

Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibiotics and antiviral agents. Its structure supports the formation of bioactive molecules with potent antimicrobial properties. Commonly employed in medicinal chemistry for constructing fused quinoline systems that exhibit enhanced binding to DNA gyrase and topoisomerase enzymes. Also utilized in research settings to design novel heterocyclic compounds with potential anticancer and anti-

Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibiotics and antiviral agents. Its structure supports the formation of bioactive molecules with potent antimicrobial properties. Commonly employed in medicinal chemistry for constructing fused quinoline systems that exhibit enhanced binding to DNA gyrase and topoisomerase enzymes. Also utilized in research settings to design novel heterocyclic compounds with potential anticancer and anti-inflammatory activities.

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...