6-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2,3,3,9,9,10,10-octamethyl-4,8-dioxa-3,9-disilaundecan-6-amine
95%
- Product Code: 124418
CAS:
35842-47-4
| Molecular Weight: | 463.92 g./mol | Molecular Formula: | C₂₂H₅₃NO₃Si₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22574795 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
Used primarily in organic synthesis as a protecting group for amines, this compound helps prevent unwanted reactions during complex chemical processes. It is particularly valuable in peptide synthesis, where selective protection and deprotection of functional groups are critical. The tert-butyldimethylsilyl (TBDMS) group provides stability under various reaction conditions, ensuring the amine remains intact until intentionally deprotected. Additionally, it finds applications in the development of pharmaceuticals and fine chemicals, where precise control over molecular structures is essential. Its robust nature makes it suitable for use in multi-step synthetic routes, enhancing efficiency and yield in targeted chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,998.00 |
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| 1.000 | 10-20 days | ฿5,400.00 |
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6-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2,3,3,9,9,10,10-octamethyl-4,8-dioxa-3,9-disilaundecan-6-amine
Used primarily in organic synthesis as a protecting group for amines, this compound helps prevent unwanted reactions during complex chemical processes. It is particularly valuable in peptide synthesis, where selective protection and deprotection of functional groups are critical. The tert-butyldimethylsilyl (TBDMS) group provides stability under various reaction conditions, ensuring the amine remains intact until intentionally deprotected. Additionally, it finds applications in the development of pharmaceuticals and fine chemicals, where precise control over molecular structures is essential. Its robust nature makes it suitable for use in multi-step synthetic routes, enhancing efficiency and yield in targeted chemical transformations.
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