2-Bromo-N,N-dimethylpyrimidin-4-amine

95%

Reagent Code: #215861
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CAS Number 1209459-27-7

science Other reagents with same CAS 1209459-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.05 g/mol
Formula C₆H₈BrN₃
badge Registry Numbers
MDL Number MFCD14702736
thermostat Physical Properties
Boiling Point 306.4±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.553±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo selective cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and central nervous system disorders. Its bromine functionality allows for easy functionalization via palladium-catalyzed reactions, making it valuable in drug discovery and optimization processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,930.00
inventory 250mg
10-20 days ฿4,970.00
inventory 1g
10-20 days ฿13,370.00
2-Bromo-N,N-dimethylpyrimidin-4-amine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo selective cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and central nervous system disorders. Its bromine functionality allows for easy functionalization

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo selective cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and central nervous system disorders. Its bromine functionality allows for easy functionalization via palladium-catalyzed reactions, making it valuable in drug discovery and optimization processes.

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