Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate
95%
Reagent
Code: #115683
CAS Number
221136-66-9
blur_circular Chemical Specifications
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Molecular Information
Weight
275.10 g/mol
Formula
C₉H₁₁BrN₂O₃
thermostat
Physical Properties
Boiling Point
338.3°C at 760 mmHg
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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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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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