Ethyl 4-chloro-6-iodoquinoline-3-carboxylate

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Reagent Code: #184572
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CAS Number 206257-60-5

science Other reagents with same CAS 206257-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.56 g/mol
Formula C₁₂H₉ClINO₂
badge Registry Numbers
MDL Number MFCD02349007
thermostat Physical Properties
Boiling Point 399.0±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.762±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl groups, enabling the construction of biologically active molecules. Also utilized in research settings for the preparation of fluorescent probes and kinase inhibitors due to the inherent photophysical properties of the quinoline core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿13,350.00
inventory 1g
10-20 days ฿19,500.00

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Ethyl 4-chloro-6-iodoquinoline-3-carboxylate
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Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl groups, enabling the construction of biologically active molecules. Also utilized in r

Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl groups, enabling the construction of biologically active molecules. Also utilized in research settings for the preparation of fluorescent probes and kinase inhibitors due to the inherent photophysical properties of the quinoline core.

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