4,4',4''-Tris(benzoyloxy)trityl Bromide [Hydroxyl Protecting Agent]
≥97%
- Product Code: 60095
CAS:
86610-66-4
| Molecular Weight: | 683.55 g./mol | Molecular Formula: | C₄₀H₂₇BrO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00010302 | |
| Melting Point: | 192-198°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a hydroxyl-protecting agent in organic synthesis. It is particularly valuable in the protection of hydroxyl groups during complex chemical reactions, ensuring that these groups remain intact while other functional groups undergo transformations. Its application is common in the synthesis of pharmaceuticals, natural products, and fine chemicals, where selective protection and deprotection of hydroxyl groups are critical. The compound’s stability and efficiency make it a preferred choice in multi-step synthetic processes, especially in peptide and carbohydrate chemistry. Additionally, it is utilized in the preparation of intermediates for drug development, where precise control over reactive sites is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,690.00 |
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| 5.000 | 10-20 days | ฿8,955.00 |
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4,4',4''-Tris(benzoyloxy)trityl Bromide [Hydroxyl Protecting Agent]
This chemical is primarily used as a hydroxyl-protecting agent in organic synthesis. It is particularly valuable in the protection of hydroxyl groups during complex chemical reactions, ensuring that these groups remain intact while other functional groups undergo transformations. Its application is common in the synthesis of pharmaceuticals, natural products, and fine chemicals, where selective protection and deprotection of hydroxyl groups are critical. The compound’s stability and efficiency make it a preferred choice in multi-step synthetic processes, especially in peptide and carbohydrate chemistry. Additionally, it is utilized in the preparation of intermediates for drug development, where precise control over reactive sites is essential.
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