5-Bromo-2,4-dimethoxypyrimidine

98.0%

Reagent Code: #143489
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CAS Number 56686-16-9

science Other reagents with same CAS 56686-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.04 g/mol
Formula C₆H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD00038016
thermostat Physical Properties
Melting Point 62-65 °C(lit.)
Boiling Point 125 °C / 17mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biologically active molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿148.50
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿1,030.00
inventory 100g
10-20 days ฿3,110.00
inventory 500g
10-20 days ฿11,730.00

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5-Bromo-2,4-dimethoxypyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biologically active molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reacti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biologically active molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

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