Trimethylsilylmethanol
98%
- Product Code: 121895
CAS:
3219-63-4
| Molecular Weight: | 104.22 g./mol | Molecular Formula: | C₄H₁₂OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00004596 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.826 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
Trimethylsilylmethanol is primarily used as a protecting group in organic synthesis, particularly for alcohols and phenols. Its ability to form stable silyl ethers makes it valuable in multi-step reactions, where temporary protection of hydroxyl groups is necessary to prevent unwanted reactions. It is also employed in the preparation of silicon-containing polymers and resins, contributing to their stability and performance. Additionally, it serves as a reagent in the modification of surfaces, enhancing hydrophobicity or enabling further functionalization. In some cases, it is utilized in the synthesis of pharmaceutical intermediates, where its unique reactivity aids in achieving specific molecular structures.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Almost Colorless Clear Liquid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $44.70 |
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| 5.000 | 10-20 days | $160.82 |
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Trimethylsilylmethanol
Trimethylsilylmethanol is primarily used as a protecting group in organic synthesis, particularly for alcohols and phenols. Its ability to form stable silyl ethers makes it valuable in multi-step reactions, where temporary protection of hydroxyl groups is necessary to prevent unwanted reactions. It is also employed in the preparation of silicon-containing polymers and resins, contributing to their stability and performance. Additionally, it serves as a reagent in the modification of surfaces, enhancing hydrophobicity or enabling further functionalization. In some cases, it is utilized in the synthesis of pharmaceutical intermediates, where its unique reactivity aids in achieving specific molecular structures.
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