N-tert-Butoxycarbonyl-N-[3-(tert-butoxycarbonylamino)propyl]glycine
98%
- Product Code: 92764
CAS:
192124-66-6
| Molecular Weight: | 332.4 g./mol | Molecular Formula: | C₁₅H₂₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797057 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in preventing unwanted reactions during the formation of peptide bonds, ensuring the correct sequence and structure of the peptide. Its tert-butoxycarbonyl (Boc) groups are particularly effective in providing stability under various reaction conditions, making it a valuable reagent in the synthesis of complex peptides and proteins. Additionally, it is utilized in the development of pharmaceuticals and biochemical research, where precise control over peptide assembly is crucial. The compound's ability to be selectively removed under mild acidic conditions further enhances its utility in multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿6,670.00 |
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| 0.200 | 10-20 days | ฿22,320.00 |
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N-tert-Butoxycarbonyl-N-[3-(tert-butoxycarbonylamino)propyl]glycine
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in preventing unwanted reactions during the formation of peptide bonds, ensuring the correct sequence and structure of the peptide. Its tert-butoxycarbonyl (Boc) groups are particularly effective in providing stability under various reaction conditions, making it a valuable reagent in the synthesis of complex peptides and proteins. Additionally, it is utilized in the development of pharmaceuticals and biochemical research, where precise control over peptide assembly is crucial. The compound's ability to be selectively removed under mild acidic conditions further enhances its utility in multi-step synthetic processes.
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