2-Amino-5-bromo-4-methylpyrimidine

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Reagent Code: #135726
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CAS Number 17321-93-6

science Other reagents with same CAS 17321-93-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.03 g/mol
Formula C₅H₆BrN₃
badge Registry Numbers
MDL Number MFCD00094469
thermostat Physical Properties
Melting Point 196-200°C
Boiling Point 345.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of pyrimidine-based compounds that can interfere with nucleic acid replication, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. The bromo and amino groups allow for further functionalization through cross-coupling reactions, enabling diverse molecular modifications in drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿253.00
inventory 5g
10-20 days ฿913.00
inventory 25g
10-20 days ฿8,270.00
inventory 100g
10-20 days ฿32,270.00

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2-Amino-5-bromo-4-methylpyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of pyrimidine-based compounds that can interfere with nucleic acid replication, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. The bromo and amino groups allow for further functionalization through cross-coupling reacti
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of pyrimidine-based compounds that can interfere with nucleic acid replication, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. The bromo and amino groups allow for further functionalization through cross-coupling reactions, enabling diverse molecular modifications in drug discovery and materials science.
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