4,8-Dibromo-2-methylquinoline

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Reagent Code: #129477
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CAS Number 1070879-55-8

science Other reagents with same CAS 1070879-55-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.98 g/mol
Formula C₁₀H₇Br₂N
badge Registry Numbers
MDL Number MFCD11505139
thermostat Physical Properties
Boiling Point 343.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.819±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of kinase inhibitors and other biologically active compounds. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to construct complex quinoline derivatives. Applied in materials science for designing electron-transport materials and fluorescent probes. Also investigated for potential antitumor and antimicrobial activities due to the bioactive nature of halogenated quinolines.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,490.00
inventory 250mg
10-20 days ฿10,990.00
inventory 1g
10-20 days ฿30,340.00

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4,8-Dibromo-2-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 kinase inhibitors and other biologically active compounds. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to construct complex quinoline derivatives. Applied in materials science for designing electron-transport materials and fluorescent probes. Also investigated for potential antitumor and antimicrobial activities due to the bioactive nat

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of kinase inhibitors and other biologically active compounds. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to construct complex quinoline derivatives. Applied in materials science for designing electron-transport materials and fluorescent probes. Also investigated for potential antitumor and antimicrobial activities due to the bioactive nature of halogenated quinolines.

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