(1-Tritylimidazol-4-yl)boronic acid
95%
- Product Code: 242086
CAS:
1900755-49-8
| Molecular Weight: | 354.21 g./mol | Molecular Formula: | C₂₂H₁₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10696629 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as a key intermediate in the synthesis of bioactive molecules, particularly in the development of pharmaceuticals targeting enzyme inhibition and receptor modulation. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex organic frameworks for drug discovery. The trityl-protected imidazole group enhances stability and solubility during synthesis, allowing selective deprotection for further functionalization. Commonly employed in the preparation of protease inhibitors and kinase modulators due to the imidazole’s role in mimicking histidine residues in enzyme substrates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,680.00 |
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| 250mg | 10-20 days | ฿10,080.00 |
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| 1g | 10-20 days | ฿22,640.00 |
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| 5g | 10-20 days | ฿60,360.00 |
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| 10g | 10-20 days | ฿118,200.00 |
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| bulk | 10-20 days | ฿0.00 |
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(1-Tritylimidazol-4-yl)boronic acid
Used as a key intermediate in the synthesis of bioactive molecules, particularly in the development of pharmaceuticals targeting enzyme inhibition and receptor modulation. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex organic frameworks for drug discovery. The trityl-protected imidazole group enhances stability and solubility during synthesis, allowing selective deprotection for further functionalization. Commonly employed in the preparation of protease inhibitors and kinase modulators due to the imidazole’s role in mimicking histidine residues in enzyme substrates.
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| Stable in pH range | - |
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