5-bromo-N-methyl-8-quinolinamine

97%

Reagent Code: #215165
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CAS Number 2304753-12-4

science Other reagents with same CAS 2304753-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.0959 g/mol
Formula C₁₀H₉BrN₂
badge Registry Numbers
MDL Number MFCD32869266
thermostat Physical Properties
Boiling Point 354.8±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.555±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and functionalizable amine group. Employed in research for designing kinase inhibitors and fluorescent probes, leveraging the bromine atom for cross-coupling reactions. Also explored in coordination chemistry as a ligand for metal complexes with potential catalytic or biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,400.00
inventory 250mg
10-20 days ฿20,800.00
inventory 1g
10-20 days ฿48,000.00
5-bromo-N-methyl-8-quinolinamine
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and functionalizable amine group. Employed in research for designing kinase inhibitors and fluorescent probes, leveraging the bromine atom for cross-coupling reactions. Also explored in coordination chemistry as a ligand for metal complexes with potential catalytic or biological activity.

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and functionalizable amine group. Employed in research for designing kinase inhibitors and fluorescent probes, leveraging the bromine atom for cross-coupling reactions. Also explored in coordination chemistry as a ligand for metal complexes with potential catalytic or biological activity.

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