2-(4-((tert-Butyldimethylsilyl)oxy)-2-methylbutan-2-yl)-3,5-dimethylphenol
95%
- Product Code: 41542
CAS:
134098-64-9
| Molecular Weight: | 322.5576 g./mol | Molecular Formula: | C₁₉H₃₄O₂Si |
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| EC Number: | MDL Number: | MFCD20268101 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities. Its tert-butyldimethylsilyl (TBDMS) group is particularly effective in safeguarding hydroxyl groups during complex chemical reactions, such as multi-step synthesis of pharmaceuticals and natural products. The steric bulk of the TBDMS group provides stability against various reaction conditions, including acidic or basic environments, while allowing selective deprotection when needed. Additionally, the compound's phenolic structure can be leveraged in the development of antioxidants or as intermediates in the synthesis of more complex phenolic compounds. Its application is also seen in the preparation of specialty chemicals where precise control over reactivity and protection of functional groups is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,036.00 |
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2-(4-((tert-Butyldimethylsilyl)oxy)-2-methylbutan-2-yl)-3,5-dimethylphenol
This compound is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities. Its tert-butyldimethylsilyl (TBDMS) group is particularly effective in safeguarding hydroxyl groups during complex chemical reactions, such as multi-step synthesis of pharmaceuticals and natural products. The steric bulk of the TBDMS group provides stability against various reaction conditions, including acidic or basic environments, while allowing selective deprotection when needed. Additionally, the compound's phenolic structure can be leveraged in the development of antioxidants or as intermediates in the synthesis of more complex phenolic compounds. Its application is also seen in the preparation of specialty chemicals where precise control over reactivity and protection of functional groups is critical.
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