5-bromo-2-chloro-4-methoxypyrimidine

95%

Reagent Code: #143994
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CAS Number 57054-92-9

science Other reagents with same CAS 57054-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.46 g/mol
Formula C₅H₄BrClN₂O
badge Registry Numbers
MDL Number MFCD03001373
inventory_2 Storage & Handling
Storage 2-8℃, light-proof, inert gas environment

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its halogenated pyrimidine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides due to its ability to modulate biological activity in target organisms.

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Test Parameter Specification
Appearance White to off-white solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿810.00
inventory 25g
10-20 days ฿3,790.00

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5-bromo-2-chloro-4-methoxypyrimidine
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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 halogenated pyrimidine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides due to its ability to modulate biologic

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its halogenated pyrimidine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides due to its ability to modulate biological activity in target organisms.

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