2-Bromo-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carbaldehyde
95%
- Product Code: 88204
CAS:
1185428-34-5
| Molecular Weight: | 356.29 g./mol | Molecular Formula: | C₁₃H₁₈BrN₃O₂Si |
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| EC Number: | MDL Number: | MFCD24848155 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of complex pharmaceutical intermediates. Its structure, featuring a bromo group and a protected aldehyde, makes it a valuable building block for constructing pyrrolopyrazine derivatives, which are often explored for their biological activity. The trimethylsilyl ethoxy methyl (SEM) group serves as a protective moiety, allowing selective reactions to occur at other sites of the molecule. This chemical is frequently employed in medicinal chemistry research to design and synthesize potential drug candidates, especially in the fields of oncology and neurology, where pyrrolopyrazine scaffolds are of significant interest. Additionally, its reactivity enables its use in cross-coupling reactions, facilitating the creation of diverse heterocyclic compounds with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,292.00 |
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| 0.250 | 10-20 days | ฿7,812.00 |
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2-Bromo-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carbaldehyde
This compound is primarily utilized in organic synthesis, particularly in the development of complex pharmaceutical intermediates. Its structure, featuring a bromo group and a protected aldehyde, makes it a valuable building block for constructing pyrrolopyrazine derivatives, which are often explored for their biological activity. The trimethylsilyl ethoxy methyl (SEM) group serves as a protective moiety, allowing selective reactions to occur at other sites of the molecule. This chemical is frequently employed in medicinal chemistry research to design and synthesize potential drug candidates, especially in the fields of oncology and neurology, where pyrrolopyrazine scaffolds are of significant interest. Additionally, its reactivity enables its use in cross-coupling reactions, facilitating the creation of diverse heterocyclic compounds with potential therapeutic applications.
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