4-bromo-2,6,8-trimethylquinoline

97%

Reagent Code: #129476
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CAS Number 1070879-60-5

science Other reagents with same CAS 1070879-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.13 g/mol
Formula C₁₂H₁₂BrN
badge Registry Numbers
MDL Number MFCD11505145
thermostat Physical Properties
Boiling Point 333.4±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.375±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors due to the quinoline core’s affinity for enzyme active sites. Its bromine substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of ligands for catalysis and in materials science for designing nitrogen-containing heterocyclic compounds with potential optoelectronic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,160.00
250mg
10-20 days ฿10,330.00
1g
10-20 days ฿32,850.00
4-bromo-2,6,8-trimethylquinoline
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors due to the quinoline core’s affinity for enzyme active sites. Its bromine substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of ligands for catalysis and in materials science for designing nitrogen-containing

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors due to the quinoline core’s affinity for enzyme active sites. Its bromine substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of ligands for catalysis and in materials science for designing nitrogen-containing heterocyclic compounds with potential optoelectronic properties.

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