Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate

95%

Reagent Code: #115683
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CAS Number 221136-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.10 g/mol
Formula C₉H₁₁BrN₂O₃
thermostat Physical Properties
Boiling Point 338.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a bromo and methyl-substituted pyrazinone ring, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The presence of the ethyl acetate group enhances its reactivity, allowing it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing diverse heterocyclic compounds. Additionally, it serves as a building block in the preparation of potential bioactive compounds, including those with antimicrobial or anticancer properties. Its versatility in chemical transformations makes it a valuable tool for researchers in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $597.52
inventory 100mg
10-20 days $299.04
Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a bromo and methyl-substituted pyrazinone ring, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The presence of the ethyl acetate group enhances its reactivity, allowing it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing diverse heterocyclic compounds. Additionally, it serves as a building block in the preparation of potential bioactive compounds, including those with antimicrobial or anticancer properties. Its versatility in chemical transformations makes it a valuable tool for researchers in medicinal chemistry and drug discovery.
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