2-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Prop-2-En-1-Ol
95%
- Product Code: 85064
CAS:
116700-73-3
| Molecular Weight: | 202.37 g./mol | Molecular Formula: | C₁₀H₂₂O₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22571041 | |
| Melting Point: | Boiling Point: | 236.2±28.0 °C(Predicted) | |
| Density: | 0.886±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for alcohols. The tert-butyldimethylsilyl (TBDMS) group shields the hydroxyl functionality during complex chemical reactions, preventing unwanted interactions. It is particularly valuable in multi-step synthesis processes, such as the production of pharmaceuticals, where selective protection and deprotection of functional groups are essential. Additionally, its stability under various reaction conditions makes it a reliable choice for synthesizing complex molecules, including natural products and fine chemicals. After the desired reactions are complete, the TBDMS group can be removed under mild conditions, restoring the original alcohol functionality without disrupting the rest of the molecule.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,808.00 |
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| 0.250 | 10-20 days | ฿5,265.00 |
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| 1.000 | 10-20 days | ฿10,530.00 |
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2-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Prop-2-En-1-Ol
This compound is primarily used in organic synthesis as a protecting group for alcohols. The tert-butyldimethylsilyl (TBDMS) group shields the hydroxyl functionality during complex chemical reactions, preventing unwanted interactions. It is particularly valuable in multi-step synthesis processes, such as the production of pharmaceuticals, where selective protection and deprotection of functional groups are essential. Additionally, its stability under various reaction conditions makes it a reliable choice for synthesizing complex molecules, including natural products and fine chemicals. After the desired reactions are complete, the TBDMS group can be removed under mild conditions, restoring the original alcohol functionality without disrupting the rest of the molecule.
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