4-Iodo-1-trityl-1H-pyrazole
≥95%
- Product Code: 119536
CAS:
191980-54-8
| Molecular Weight: | 436.29 g./mol | Molecular Formula: | C₂₂H₁₇IN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23135653 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, particularly in the synthesis of pyrazole derivatives, which are known for their biological activities. The trityl group provides protection for the nitrogen atom during reactions, allowing for selective modifications at other positions of the pyrazole ring. Additionally, the iodine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse compounds for drug discovery and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿468.00 |
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| 0.250 | 10-20 days | ฿783.00 |
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| 1.000 | 10-20 days | ฿2,322.00 |
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4-Iodo-1-trityl-1H-pyrazole
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, particularly in the synthesis of pyrazole derivatives, which are known for their biological activities. The trityl group provides protection for the nitrogen atom during reactions, allowing for selective modifications at other positions of the pyrazole ring. Additionally, the iodine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse compounds for drug discovery and material science applications.
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