(R)-2-((tert-Butoxycarbonyl)amino)-3-(ethylthio)propanoic acid
97%
- Product Code: 37460
CAS:
16947-82-3
| Molecular Weight: | 249.3272 g./mol | Molecular Formula: | C₁₀H₁₉NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076919 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of peptides and peptidomimetics, where it serves as a building block for introducing specific amino acid structures into larger molecules. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during peptide coupling reactions, while the ethylthio moiety can be leveraged for further functionalization or as a precursor for more complex sulfur-containing compounds. It is particularly valuable in medicinal chemistry for designing drug candidates targeting enzymes or receptors that interact with sulfur-based functional groups. Additionally, it finds use in research settings for studying the role of thioether linkages in protein structure and function.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,179.00 |
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(R)-2-((tert-Butoxycarbonyl)amino)-3-(ethylthio)propanoic acid
This chemical is primarily utilized in the synthesis of peptides and peptidomimetics, where it serves as a building block for introducing specific amino acid structures into larger molecules. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during peptide coupling reactions, while the ethylthio moiety can be leveraged for further functionalization or as a precursor for more complex sulfur-containing compounds. It is particularly valuable in medicinal chemistry for designing drug candidates targeting enzymes or receptors that interact with sulfur-based functional groups. Additionally, it finds use in research settings for studying the role of thioether linkages in protein structure and function.
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