5-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Pyrrolidin-2-One
95%
- Product Code: 63706
CAS:
177911-57-8
| Molecular Weight: | 229.39 g./mol | Molecular Formula: | C₁₁H₂₃NO₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23135503 | |
| Melting Point: | Boiling Point: | 307.6±15.0 °C(Predicted) | |
| Density: | 0.942±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities. Its tert-butyldimethylsilyl (TBDMS) group is particularly effective in safeguarding alcohols during complex multi-step reactions, ensuring that the hydroxyl group remains intact while other parts of the molecule undergo chemical transformations. This compound is especially valuable in the synthesis of pharmaceuticals and natural products, where selective protection and deprotection of functional groups are crucial. Additionally, its pyrrolidin-2-one moiety can serve as a building block in the construction of more complex heterocyclic compounds, which are often key intermediates in drug development. Its stability under various reaction conditions makes it a reliable choice for chemists working on intricate synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €128.22 |
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| 0.250 | 10-20 days | €249.31 |
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| 1.000 | 10-20 days | €498.62 |
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5-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Pyrrolidin-2-One
This chemical is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities. Its tert-butyldimethylsilyl (TBDMS) group is particularly effective in safeguarding alcohols during complex multi-step reactions, ensuring that the hydroxyl group remains intact while other parts of the molecule undergo chemical transformations. This compound is especially valuable in the synthesis of pharmaceuticals and natural products, where selective protection and deprotection of functional groups are crucial. Additionally, its pyrrolidin-2-one moiety can serve as a building block in the construction of more complex heterocyclic compounds, which are often key intermediates in drug development. Its stability under various reaction conditions makes it a reliable choice for chemists working on intricate synthetic pathways.
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