Ethyl 4-chloro-8-fluoroquinoline-3-carboxylate

98%

Reagent Code: #47234
fingerprint
CAS Number 56824-90-9

science Other reagents with same CAS 56824-90-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.6600 g/mol
Formula C₁₂H₉ClFNO₂
badge Registry Numbers
MDL Number MFCD00173364
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both chloro and fluoro substituents on the quinoline ring, makes it a valuable precursor for developing drugs, particularly antibiotics and antimicrobial agents. Researchers often employ it in the creation of quinolone derivatives, which are known for their efficacy in treating bacterial infections. Additionally, its carboxylate group allows for further functionalization, enabling the production of compounds with potential therapeutic applications in areas such as cancer treatment and anti-inflammatory drugs. Its role in medicinal chemistry underscores its importance in advancing drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,430.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 4-chloro-8-fluoroquinoline-3-carboxylate
No image available

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both chloro and fluoro substituents on the quinoline ring, makes it a valuable precursor for developing drugs, particularly antibiotics and antimicrobial agents. Researchers often employ it in the creation of quinolone derivatives, which are known for their efficacy in treating bacterial infections. Additionally,

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both chloro and fluoro substituents on the quinoline ring, makes it a valuable precursor for developing drugs, particularly antibiotics and antimicrobial agents. Researchers often employ it in the creation of quinolone derivatives, which are known for their efficacy in treating bacterial infections. Additionally, its carboxylate group allows for further functionalization, enabling the production of compounds with potential therapeutic applications in areas such as cancer treatment and anti-inflammatory drugs. Its role in medicinal chemistry underscores its importance in advancing drug discovery and development.

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...