6-Methoxy-2-(trifluoromethyl)quinolin-4-ol

95%

Reagent Code: #210505
fingerprint
CAS Number 1701-21-9

science Other reagents with same CAS 1701-21-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.18 g/mol
Formula C₁₁H₈F₃NO₂
badge Registry Numbers
MDL Number MFCD11855897
thermostat Physical Properties
Melting Point 275-277 °C
Boiling Point 339.9±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.407±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. Commonly applied in the development of antimalarial and anticancer agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its trifluoromethyl and methoxy groups contribute to lipophilicity and electron-donating effects, making it valuable in optimizing lead compounds during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,590.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Methoxy-2-(trifluoromethyl)quinolin-4-ol
No image available

Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. Commonly applied in the development of antimalarial and anticancer agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its trifluoromethyl and methoxy groups contribute to lipophilicity and electron-donating effects, making i

Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. Commonly applied in the development of antimalarial and anticancer agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its trifluoromethyl and methoxy groups contribute to lipophilicity and electron-donating effects, making it valuable in optimizing lead compounds during drug discovery.

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...