Fmoc-D-2-Cyanophe
≥95%
- Product Code: 189797
CAS:
401620-74-4
| Molecular Weight: | 412.45 g./mol | Molecular Formula: | C₂₅H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863770 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used primarily in solid-phase peptide synthesis, this compound serves as a chiral building block for incorporating modified amino acids into peptide chains. The Fmoc group enables orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during repetitive synthesis cycles. The D-configuration and cyano substituent introduce structural rigidity and influence peptide conformation, making it valuable in designing peptidomimetics and bioactive analogs with enhanced metabolic stability. It is also employed in the development of enzyme inhibitors and probes for studying protein–protein interactions. Its nitrile functionality can participate in click chemistry or be further derivatized, expanding its utility in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $571.80 |
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Fmoc-D-2-Cyanophe
Used primarily in solid-phase peptide synthesis, this compound serves as a chiral building block for incorporating modified amino acids into peptide chains. The Fmoc group enables orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during repetitive synthesis cycles. The D-configuration and cyano substituent introduce structural rigidity and influence peptide conformation, making it valuable in designing peptidomimetics and bioactive analogs with enhanced metabolic stability. It is also employed in the development of enzyme inhibitors and probes for studying protein–protein interactions. Its nitrile functionality can participate in click chemistry or be further derivatized, expanding its utility in medicinal chemistry and drug discovery.
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