7-bromo-6-methyl-2-phenyl-1H-quinolin-4-one

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Reagent Code: #129326
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CAS Number 1189105-49-4

science Other reagents with same CAS 1189105-49-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.18 g/mol
Formula C₁₆H₁₂BrNO
thermostat Physical Properties
Boiling Point 487.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.475±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing biologically active quinoline derivatives. Shows potential in the development of anticancer agents due to its ability to inhibit specific kinase enzymes involved in tumor growth. Also investigated for antimicrobial properties, particularly against resistant bacterial strains. Its structure allows for easy modification, making it valuable in optimizing drug candidates for improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,600.00
inventory 500mg
10-20 days ฿24,410.00

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7-bromo-6-methyl-2-phenyl-1H-quinolin-4-one
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Used in pharmaceutical research as a key intermediate for synthesizing biologically active quinoline derivatives. Shows potential in the development of anticancer agents due to its ability to inhibit specific kinase enzymes involved in tumor growth. Also investigated for antimicrobial properties, particularly against resistant bacterial strains. Its structure allows for easy modification, making it valuable in optimizing drug candidates for improved efficacy and selectivity.
Used in pharmaceutical research as a key intermediate for synthesizing biologically active quinoline derivatives. Shows potential in the development of anticancer agents due to its ability to inhibit specific kinase enzymes involved in tumor growth. Also investigated for antimicrobial properties, particularly against resistant bacterial strains. Its structure allows for easy modification, making it valuable in optimizing drug candidates for improved efficacy and selectivity.
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