4-Bromo-5-(trifluoromethyl)pyridin-2-amine

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Reagent Code: #140750
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CAS Number 1227599-92-9

science Other reagents with same CAS 1227599-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.01 g/mol
Formula C₆H₄N₂F₃Br
badge Registry Numbers
MDL Number MFCD16606114
thermostat Physical Properties
Boiling Point 262.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.790±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high potency and specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the stability and electron-withdrawing nature of the trifluoromethyl group.

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inventory 1g
10-20 days ฿106,010.00

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4-Bromo-5-(trifluoromethyl)pyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high potency and specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and he

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high potency and specificity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the stability and electron-withdrawing nature of the trifluoromethyl group.

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