4-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
95%
- Product Code: 196435
CAS:
220299-49-0
| Molecular Weight: | 324.23 g./mol | Molecular Formula: | C₉H₁₇IN₂OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20483624 | |
| Melting Point: | Boiling Point: | 315.0±27.0 °C(Predicted) | |
| Density: | 1.44±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a protected pyrazole derivative in organic synthesis, particularly in pharmaceutical and agrochemical research. The SEM protecting group (trimethylsilylethoxymethyl) stabilizes the pyrazole nitrogen during multi-step reactions, allowing selective functionalization at other sites. The iodine atom serves as a handle for cross-coupling reactions such as Suzuki or Sonogashira couplings, enabling the construction of complex heterocyclic systems. Commonly employed in the development of bioactive molecules where pyrazole scaffolds are key structural elements.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿30,170.00 |
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| 1g | 10-20 days | ฿38,790.00 |
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4-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
Used as a protected pyrazole derivative in organic synthesis, particularly in pharmaceutical and agrochemical research. The SEM protecting group (trimethylsilylethoxymethyl) stabilizes the pyrazole nitrogen during multi-step reactions, allowing selective functionalization at other sites. The iodine atom serves as a handle for cross-coupling reactions such as Suzuki or Sonogashira couplings, enabling the construction of complex heterocyclic systems. Commonly employed in the development of bioactive molecules where pyrazole scaffolds are key structural elements.
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