1-(2-Methoxyquinolin-3-yl)ethan-1-one

95%

Reagent Code: #209468
fingerprint
CAS Number 850171-06-1

science Other reagents with same CAS 850171-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.22 g/mol
Formula C₁₂H₁₁NO₂
badge Registry Numbers
MDL Number MFCD28140211
thermostat Physical Properties
Melting Point 110-112 °C
Boiling Point 318.3±22.0 °C
inventory_2 Storage & Handling
Density 1.167±0.06 g/cm3
Storage 2-8°C

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds. Shows potential in the development of antimalarial and antimicrobial agents due to the quinoline core. Also explored in the design of kinase inhibitors for cancer therapy. Its methoxy and ketone functional groups allow for easy modification in medicinal chemistry workflows. Employed in fluorescence studies owing to the inherent photophysical properties of the quinoline ring, making it useful in probing biological systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,610.00
inventory 1g
10-20 days ฿12,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(2-Methoxyquinolin-3-yl)ethan-1-one
No image available

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds. Shows potential in the development of antimalarial and antimicrobial agents due to the quinoline core. Also explored in the design of kinase inhibitors for cancer therapy. Its methoxy and ketone functional groups allow for easy modification in medicinal chemistry workflows. Employed in fluorescence studies owing to the inherent photophysical properties of the quinoline ring, making it useful in probing biol

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds. Shows potential in the development of antimalarial and antimicrobial agents due to the quinoline core. Also explored in the design of kinase inhibitors for cancer therapy. Its methoxy and ketone functional groups allow for easy modification in medicinal chemistry workflows. Employed in fluorescence studies owing to the inherent photophysical properties of the quinoline ring, making it useful in probing biological systems.

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...