4-Bromo-6-ethyl-2-methylquinoline

98%

Reagent Code: #129228
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CAS Number 1070879-44-5

science Other reagents with same CAS 1070879-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.13 g/mol
Formula C₁₂H₁₂BrN
badge Registry Numbers
MDL Number MFCD11505128
thermostat Physical Properties
Boiling Point 331.0±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.373±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex quinoline-based compounds with potential biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds, enabling the introduction of various functional groups. Also utilized in the research of kinase inhibitors and other bioactive molecules due to the quinoline core’s affinity for biological targets. Serves as a building block in medicinal chemistry for designing compounds with antimicrobial, anti-inflammatory, or anticancer properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿10,190.00
1g
10-20 days ฿30,340.00
4-Bromo-6-ethyl-2-methylquinoline
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex quinoline-based compounds with potential biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds, enabling the introduction of various functional groups. Also utilized in the research of kinase inhibitors and other bioactive molecules due to the quinoline core

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex quinoline-based compounds with potential biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds, enabling the introduction of various functional groups. Also utilized in the research of kinase inhibitors and other bioactive molecules due to the quinoline core’s affinity for biological targets. Serves as a building block in medicinal chemistry for designing compounds with antimicrobial, anti-inflammatory, or anticancer properties.

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