Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate
95%
- Product Code: 115683
CAS:
221136-66-9
| Molecular Weight: | 275.10 g./mol | Molecular Formula: | C₉H₁₁BrN₂O₃ |
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| Melting Point: | Boiling Point: | 338.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $402.91 |
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| 0.250 | 10-20 days | $805.08 |
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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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