(2S)-2-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]diphenylmethyl]pyrrolidine
≥98%,99%e.e.
- Product Code: 65683
CAS:
864466-71-7
| Molecular Weight: | 367.6 g./mol | Molecular Formula: | C₂₃H₃₃NOSi |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols and amines. Its sterically bulky structure helps shield sensitive functional groups during complex reactions, particularly in the synthesis of pharmaceuticals and natural products. The compound is often employed in the preparation of chiral molecules, where selective protection and deprotection are crucial for achieving the desired stereochemistry. Additionally, it finds application in the development of peptide-based drugs, where it aids in controlling the reactivity of specific amino groups, ensuring the integrity of the peptide chain during synthesis. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white light yellow powder, Fine crystals with lumps |
| 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 | ฿16,350.00 |
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(2S)-2-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]diphenylmethyl]pyrrolidine
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols and amines. Its sterically bulky structure helps shield sensitive functional groups during complex reactions, particularly in the synthesis of pharmaceuticals and natural products. The compound is often employed in the preparation of chiral molecules, where selective protection and deprotection are crucial for achieving the desired stereochemistry. Additionally, it finds application in the development of peptide-based drugs, where it aids in controlling the reactivity of specific amino groups, ensuring the integrity of the peptide chain during synthesis. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes.
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