4-[(7-Chloroquinolin-4-yl)oxy]-3-fluoroaniline

95%

Reagent Code: #130277
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CAS Number 1094937-81-1

science Other reagents with same CAS 1094937-81-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.7 g/mol
Formula C₁₅H₁₀ClFN₂O
badge Registry Numbers
MDL Number MFCD12572239
thermostat Physical Properties
Boiling Point 441.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.402±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used primarily as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the creation of compounds that inhibit hemozoin formation in Plasmodium species, thereby disrupting the parasite's ability to detoxify heme during red blood cell infection. Also explored for potential antiviral and anticancer applications due to its ability to intercalate into nucleic acids and interfere with cellular replication processes. Employed in research settings to design novel bioactive molecules with improved pharmacokinetic and resistance profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,650.00

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4-[(7-Chloroquinolin-4-yl)oxy]-3-fluoroaniline
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Used primarily as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the creation of compounds that inhibit hemozoin formation in Plasmodium species, thereby disrupting the parasite's ability to detoxify heme during red blood cell infection. Also explored for potential antiviral and anticancer applications due to its ability to intercalate into nucleic acids and interfere with cellular replication processes

Used primarily as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of quinoline-based pharmaceuticals. Its structure supports the creation of compounds that inhibit hemozoin formation in Plasmodium species, thereby disrupting the parasite's ability to detoxify heme during red blood cell infection. Also explored for potential antiviral and anticancer applications due to its ability to intercalate into nucleic acids and interfere with cellular replication processes. Employed in research settings to design novel bioactive molecules with improved pharmacokinetic and resistance profiles.

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