(1-Trityl-1H-Pyrazol-4-Yl)Methanol
95%
- Product Code: 84768
CAS:
88529-69-5
| Molecular Weight: | 340.42 g./mol | Molecular Formula: | C₂₃H₂₀N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29917021 | |
| Melting Point: | Boiling Point: | 544.7±50.0 °C(Predicted) | |
| Density: | 1.10±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
(1-Trityl-1H-Pyrazol-4-Yl)Methanol is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a trityl-protected pyrazole moiety, makes it valuable in the development of pharmaceuticals and bioactive compounds. It is often employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it serves as a building block for designing drug candidates. The trityl group provides stability during reactions, allowing selective modifications to the pyrazole ring. This compound is also explored in the creation of ligands for metal-catalyzed reactions, contributing to advancements in catalysis and material science. Its applications extend to the study of enzyme inhibitors and receptor modulators, aiding in the discovery of new therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,126.00 |
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| 0.250 | 10-20 days | ฿18,000.00 |
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| 1.000 | 10-20 days | ฿36,000.00 |
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(1-Trityl-1H-Pyrazol-4-Yl)Methanol
(1-Trityl-1H-Pyrazol-4-Yl)Methanol is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a trityl-protected pyrazole moiety, makes it valuable in the development of pharmaceuticals and bioactive compounds. It is often employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it serves as a building block for designing drug candidates. The trityl group provides stability during reactions, allowing selective modifications to the pyrazole ring. This compound is also explored in the creation of ligands for metal-catalyzed reactions, contributing to advancements in catalysis and material science. Its applications extend to the study of enzyme inhibitors and receptor modulators, aiding in the discovery of new therapeutic agents.
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