Methyl 5-bromopyrimidine-2-carboxylate

95%

Reagent Code: #205663
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CAS Number 89581-38-4

science Other reagents with same CAS 89581-38-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD11111606
thermostat Physical Properties
Melting Point 149°C(lit.)
Boiling Point 314.4±34.0 °C(Predicted)
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 other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the construction of complex molecules for drug discovery research. Also utilized in agrochemicals for the design of 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 ฿630.00
inventory 5g
10-20 days ฿2,850.00
inventory 25g
10-20 days ฿9,350.00

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Methyl 5-bromopyrimidine-2-carboxylate
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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 building pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the construction of complex molecules for drug discovery research. Also uti
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 building pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the construction of complex molecules for drug discovery research. Also utilized in agrochemicals for the design of novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.
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