5-Bromo-N-methylpyrimidin-4-amine

≥95%

Reagent Code: #148638
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CAS Number 56181-38-5

science Other reagents with same CAS 56181-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.03 g/mol
Formula C₅H₆BrN₃
badge Registry Numbers
MDL Number MFCD03861147
thermostat Physical Properties
Boiling Point 294.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key 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 cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its bromine functionality allows for selective functionalization via palladium-catalyzed reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,760.00
inventory 250mg
10-20 days ฿10,930.00
inventory 1g
10-20 days ฿27,300.00

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5-Bromo-N-methylpyrimidin-4-amine
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Used as a key 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 cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its bromine functionality allow

Used as a key 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 cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its bromine functionality allows for selective functionalization via palladium-catalyzed reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery.

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