2-amino-3-[(tert-butyldiphenylsilyl)oxy]-2-methylpropan-1-ol
95%
- Product Code: 85175
CAS:
280753-14-2
| Molecular Weight: | 343.54 g./mol | Molecular Formula: | C₂₀H₂₉NO₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30527952 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas, protected from light |
Product Description:
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols, particularly in the preparation of complex molecules. The tert-butyldiphenylsilyl (TBDPS) group is highly stable under various reaction conditions, making it suitable for multi-step synthetic processes. It is often employed in the synthesis of pharmaceuticals, natural products, and fine chemicals where selective protection and deprotection of hydroxyl groups are required. Additionally, its steric bulk helps in directing regioselective reactions, enhancing the efficiency of synthetic pathways. The compound is also used in the development of chiral intermediates, aiding in the production of enantiomerically pure substances.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,300.00 |
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| 1.000 | 10-20 days | ฿25,000.00 |
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2-amino-3-[(tert-butyldiphenylsilyl)oxy]-2-methylpropan-1-ol
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols, particularly in the preparation of complex molecules. The tert-butyldiphenylsilyl (TBDPS) group is highly stable under various reaction conditions, making it suitable for multi-step synthetic processes. It is often employed in the synthesis of pharmaceuticals, natural products, and fine chemicals where selective protection and deprotection of hydroxyl groups are required. Additionally, its steric bulk helps in directing regioselective reactions, enhancing the efficiency of synthetic pathways. The compound is also used in the development of chiral intermediates, aiding in the production of enantiomerically pure substances.
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