3-Quinolinol, 4-bromo-2-phenyl-

95%

Reagent Code: #228367
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CAS Number 1197391-19-7

science Other reagents with same CAS 1197391-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.15 g/mol
Formula C₁₅H₁₀BrNO
badge Registry Numbers
MDL Number MFCD26127443
thermostat Physical Properties
Boiling Point 398.1±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.526±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antimalarial and anticancer agents. Its bromo and phenyl substituents make it valuable in cross-coupling reactions for constructing complex organic molecules. Also employed in research for developing novel heterocyclic compounds with biological activity. Shows potential in materials science for designing organic semiconductors and fluorescent probes due to its conjugated structure.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿96,000.00

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3-Quinolinol, 4-bromo-2-phenyl-
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antimalarial and anticancer agents. Its bromo and phenyl substituents make it valuable in cross-coupling reactions for constructing complex organic molecules. Also employed in research for developing novel heterocyclic compounds with biological activity. Shows potential in materials science for designing organic semiconductors and fluorescent probes due to its conjugated structure.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antimalarial and anticancer agents. Its bromo and phenyl substituents make it valuable in cross-coupling reactions for constructing complex organic molecules. Also employed in research for developing novel heterocyclic compounds with biological activity. Shows potential in materials science for designing organic semiconductors and fluorescent probes due to its conjugated structure.

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