7-((2-(Trimethylsilyl)ethoxy)methyl)-7H-imidazo[1,2-c]pyrrolo[3,2-e]pyrimidine
95%
- Product Code: 124446
CAS:
1404299-74-6
| Molecular Weight: | 288.43 g./mol | Molecular Formula: | C₁₄H₂₀N₄OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30828795 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in organic synthesis and medicinal chemistry as a protected intermediate for the development of complex molecules. Its structure, featuring a trimethylsilyl ether group, makes it valuable in protecting sensitive functional groups during multi-step synthetic processes. It is particularly useful in the synthesis of heterocyclic compounds, which are often key components in pharmaceuticals and biologically active agents. The compound’s stability and reactivity allow it to serve as a building block in the creation of potential drug candidates, especially in the field of oncology and antiviral research. Its application is critical in enabling precise chemical transformations while minimizing unwanted side reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,040.00 |
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7-((2-(Trimethylsilyl)ethoxy)methyl)-7H-imidazo[1,2-c]pyrrolo[3,2-e]pyrimidine
This chemical is primarily used in organic synthesis and medicinal chemistry as a protected intermediate for the development of complex molecules. Its structure, featuring a trimethylsilyl ether group, makes it valuable in protecting sensitive functional groups during multi-step synthetic processes. It is particularly useful in the synthesis of heterocyclic compounds, which are often key components in pharmaceuticals and biologically active agents. The compound’s stability and reactivity allow it to serve as a building block in the creation of potential drug candidates, especially in the field of oncology and antiviral research. Its application is critical in enabling precise chemical transformations while minimizing unwanted side reactions.
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