4-Nitro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
95%
- Product Code: 124329
CAS:
1260160-79-9
| Molecular Weight: | 243.34 g./mol | Molecular Formula: | C₉H₁₇N₃O₃Si |
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| EC Number: | MDL Number: | MFCD25957287 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a protected intermediate for pyrazole derivatives. Its structure, featuring a nitro group and a trimethylsilyl-protected hydroxymethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group can be reduced to an amine, enabling further functionalization, while the protecting group can be removed under mild conditions to regenerate the reactive hydroxymethyl functionality. This versatility allows for the creation of complex molecules, particularly in the synthesis of biologically active compounds such as inhibitors or ligands for therapeutic targets. Additionally, its stability and reactivity make it a useful building block in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿24,336.00 |
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| 0.250 | 10-20 days | ฿45,630.00 |
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4-Nitro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
This compound is primarily utilized in organic synthesis as a protected intermediate for pyrazole derivatives. Its structure, featuring a nitro group and a trimethylsilyl-protected hydroxymethyl group, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group can be reduced to an amine, enabling further functionalization, while the protecting group can be removed under mild conditions to regenerate the reactive hydroxymethyl functionality. This versatility allows for the creation of complex molecules, particularly in the synthesis of biologically active compounds such as inhibitors or ligands for therapeutic targets. Additionally, its stability and reactivity make it a useful building block in medicinal chemistry research.
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