N,O-Bis(tert-butyldimethylsilyl)acetamide [tert-Butyldimethylsilylating Agent]
>95.0%(GC)
- Product Code: 77621
CAS:
82112-21-8
| Molecular Weight: | 287.59 g./mol | Molecular Formula: | C₁₄H₃₃NOSi₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321138 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
N,O-Bis(tert-butyldimethylsilyl)acetamide is widely used as a tert-butyldimethylsilylating agent in organic synthesis. Its primary application is in the protection of hydroxyl and amino groups during complex chemical reactions. This compound is particularly valuable in the synthesis of sensitive molecules, such as natural products and pharmaceuticals, where selective protection and deprotection of functional groups are crucial. It reacts efficiently with alcohols, phenols, and amines to form stable tert-butyldimethylsilyl (TBDMS) ethers or amines, which are resistant to a variety of reaction conditions. This allows chemists to perform multi-step transformations without compromising the integrity of the protected groups. Additionally, it is often employed in carbohydrate chemistry, peptide synthesis, and the preparation of nucleosides, where precise control over reactivity is essential. The compound’s high selectivity and efficiency make it a preferred choice in advanced synthetic strategies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,060.00 |
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N,O-Bis(tert-butyldimethylsilyl)acetamide [tert-Butyldimethylsilylating Agent]
N,O-Bis(tert-butyldimethylsilyl)acetamide is widely used as a tert-butyldimethylsilylating agent in organic synthesis. Its primary application is in the protection of hydroxyl and amino groups during complex chemical reactions. This compound is particularly valuable in the synthesis of sensitive molecules, such as natural products and pharmaceuticals, where selective protection and deprotection of functional groups are crucial. It reacts efficiently with alcohols, phenols, and amines to form stable tert-butyldimethylsilyl (TBDMS) ethers or amines, which are resistant to a variety of reaction conditions. This allows chemists to perform multi-step transformations without compromising the integrity of the protected groups. Additionally, it is often employed in carbohydrate chemistry, peptide synthesis, and the preparation of nucleosides, where precise control over reactivity is essential. The compound’s high selectivity and efficiency make it a preferred choice in advanced synthetic strategies.
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