(S)-11-Benzyl-1-(9H-fluoren-9-yl)-3,6,9,12,15-pentaoxo-2,18-dioxa-4,7,10,13,16-pentaazaicosan-20-oic acid
95%
- Product Code: 232485
CAS:
2264011-98-3
| Molecular Weight: | 645.66 g./mol | Molecular Formula: | C₃₃H₃₅N₅O₉ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 1107.2±65.0 °C(Predicted) | |
| Density: | 1.339±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, Sealed, Dry |
Product Description:
Used in peptide synthesis as a chiral building block, particularly in the preparation of complex organic molecules requiring stereochemical control. Its structure supports the introduction of fluorenylmethyloxycarbonyl (Fmoc) protection, making it valuable in solid-phase peptide synthesis. The compound facilitates the stepwise assembly of peptides by enabling selective deprotection and coupling reactions. It is also employed in the development of bioactive peptides and peptidomimetics for pharmaceutical research, where precise spatial arrangement of functional groups is critical for biological activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft120,290.84 |
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| 1.000 | 10-20 days | Ft553,902.21 |
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(S)-11-Benzyl-1-(9H-fluoren-9-yl)-3,6,9,12,15-pentaoxo-2,18-dioxa-4,7,10,13,16-pentaazaicosan-20-oic acid
Used in peptide synthesis as a chiral building block, particularly in the preparation of complex organic molecules requiring stereochemical control. Its structure supports the introduction of fluorenylmethyloxycarbonyl (Fmoc) protection, making it valuable in solid-phase peptide synthesis. The compound facilitates the stepwise assembly of peptides by enabling selective deprotection and coupling reactions. It is also employed in the development of bioactive peptides and peptidomimetics for pharmaceutical research, where precise spatial arrangement of functional groups is critical for biological activity.
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