8-Bromo-2-chloro-7-fluoroquinoline

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Reagent Code: #150775
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CAS Number 1152781-66-2

science Other reagents with same CAS 1152781-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.49 g/mol
Formula C₉H₄BrClFN
badge Registry Numbers
MDL Number MFCD21603645
thermostat Physical Properties
Boiling Point 325.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.746±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its halogenated quinoline structure enables selective functionalization, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, it supports the creation of complex drug candidates. Also explored in agrochemical research for designing novel active ingredients with improved stability and target specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,840.00
inventory 250mg
10-20 days ฿13,200.00
inventory 1g
10-20 days ฿37,500.00

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8-Bromo-2-chloro-7-fluoroquinoline
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its halogenated quinoline structure enables selective functionalization, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, it supports the creation of complex drug candidates. Also explored in agrochemical research

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its halogenated quinoline structure enables selective functionalization, making it valuable in medicinal chemistry for constructing bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, it supports the creation of complex drug candidates. Also explored in agrochemical research for designing novel active ingredients with improved stability and target specificity.

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