6-Bromo-4-chloro-7-fluoro-3-nitroquinoline

95%

Reagent Code: #145627
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CAS Number 853908-81-3

science Other reagents with same CAS 853908-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.49 g/mol
Formula C₉H₃BrClFN₂O₂
thermostat Physical Properties
Boiling Point 387.0±37.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds with potential anticancer and anti-inflammatory properties. Due to the presence of multiple halogen atoms, it serves as a versatile building block in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,740.00
inventory 100mg
10-20 days ฿6,610.00

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6-Bromo-4-chloro-7-fluoro-3-nitroquinoline
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds with potential anticancer and anti-inflammatory properties. Due to the presence of multiple halogen atoms, it serves as a ve

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds with potential anticancer and anti-inflammatory properties. Due to the presence of multiple halogen atoms, it serves as a versatile building block in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations.

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