6-Bromo-N-methylquinolin-4-amine

≥95%

Reagent Code: #148805
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CAS Number 916812-31-2

science Other reagents with same CAS 916812-31-2

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scatter_plot Molecular Information
Weight 237.10 g/mol
Formula C₁₀H₉BrN₂
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MDL Number MFCD14705170
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex quinoline-based structures. Its bromine functionality allows for palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in drug discovery and optimization. Also employed in the preparation of fluorescent probes and dyes owing to the inherent photophysical properties of the quinoline core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,350.00
inventory 250mg
10-20 days ฿7,700.00
inventory 1g
10-20 days ฿21,160.00

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6-Bromo-N-methylquinolin-4-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex quinoline-based structures. Its bromine functionality allows for palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in drug discovery and optimization. Also employed in the

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex quinoline-based structures. Its bromine functionality allows for palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in drug discovery and optimization. Also employed in the preparation of fluorescent probes and dyes owing to the inherent photophysical properties of the quinoline core.

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