5-bromo-2-chloro-4-(methylthio)pyrimidine

98%

Reagent Code: #143995
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CAS Number 59549-51-8

science Other reagents with same CAS 59549-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.52 g/mol
Formula C₅H₄BrClN₂S
badge Registry Numbers
MDL Number MFCD07781218
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 kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,040.00
inventory 5g
10-20 days ฿4,660.00
inventory 10g
10-20 days ฿9,280.00
inventory 25g
10-20 days ฿20,160.00

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5-bromo-2-chloro-4-(methylthio)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the creation of diverse compound libraries for drug discovery. Also util

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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