2-Aminoquinoline-4-carboxylic acid

95%

Reagent Code: #130875
fingerprint
CAS Number 157915-68-9

science Other reagents with same CAS 157915-68-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.18 g/mol
Formula C₁₀H₈N₂O₂
badge Registry Numbers
MDL Number MFCD07186432
thermostat Physical Properties
Melting Point 362 °C(decomp)
Boiling Point 417.4±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.430±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the formation of biologically active compounds that target parasite metabolism. Also employed in research for developing new antimicrobial and anticancer agents due to its ability to interact with enzyme systems and metal ions in biological environments. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Aminoquinoline-4-carboxylic acid
No image available

Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the formation of biologically active compounds that target parasite metabolism. Also employed in research for developing new antimicrobial and anticancer agents due to its ability to interact with enzyme systems and metal ions in biological environments. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and s

Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the formation of biologically active compounds that target parasite metabolism. Also employed in research for developing new antimicrobial and anticancer agents due to its ability to interact with enzyme systems and metal ions in biological environments. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

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...