8-Bromo-4-methylquinoline

95%

Reagent Code: #151624
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CAS Number 172939-50-3

science Other reagents with same CAS 172939-50-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.08 g/mol
Formula C₁₀H₈BrN
badge Registry Numbers
MDL Number MFCD12024579
thermostat Physical Properties
Boiling Point 315.773 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the presence of reactive bromine at the 8-position and the electron-rich quinoline ring. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also investigated for its potential in medicinal chemistry for designing kinase inhibitors and antimicrobial agents. Its lipophilic nature enhances cell membrane permeability, making it suitable for drug design targeting intracellular enzymes.

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Test Parameter Specification
Appearance White to light brown solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,980.00
inventory 250mg
10-20 days ฿4,600.00

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8-Bromo-4-methylquinoline
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the presence of reactive bromine at the 8-position and the electron-rich quinoline ring. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also investigated for its potential in medicinal chemistry for designing kinase inhibitors and antimicrobial agents. Its lipophilic nature enhances cell

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the presence of reactive bromine at the 8-position and the electron-rich quinoline ring. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also investigated for its potential in medicinal chemistry for designing kinase inhibitors and antimicrobial agents. Its lipophilic nature enhances cell membrane permeability, making it suitable for drug design targeting intracellular enzymes.

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