O-Benzyl-N-(tert-butoxycarbonyl)-D-serine
≥98%
- Product Code: 76589
CAS:
47173-80-8
| Molecular Weight: | 295.34 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038248 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected form of serine, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality, and the benzyl group protects the hydroxyl group during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in the production of complex peptides, where selective deprotection can be achieved without disrupting other sensitive functional groups. It is also employed in the development of biologically active molecules, such as enzyme inhibitors and receptor agonists, due to its ability to maintain structural integrity under various reaction conditions. Additionally, it is utilized in research laboratories for studying peptide structure-activity relationships and in the preparation of custom peptides for therapeutic and diagnostic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Specific rotation a20D C2 EtOH80 | -21.0--18.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿350.00 |
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| 5.000 | 10-20 days | ฿1,040.00 |
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| 25.000 | 10-20 days | ฿4,940.00 |
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O-Benzyl-N-(tert-butoxycarbonyl)-D-serine
This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected form of serine, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality, and the benzyl group protects the hydroxyl group during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in the production of complex peptides, where selective deprotection can be achieved without disrupting other sensitive functional groups. It is also employed in the development of biologically active molecules, such as enzyme inhibitors and receptor agonists, due to its ability to maintain structural integrity under various reaction conditions. Additionally, it is utilized in research laboratories for studying peptide structure-activity relationships and in the preparation of custom peptides for therapeutic and diagnostic applications.
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