(2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(2-oxopiperidin-1-yl)pyrrolidine-2-carboxylic acid
98%
- Product Code: 232509
CAS:
2029092-01-9
| Molecular Weight: | 434.48 g./mol | Molecular Formula: | C₂₅H₂₆N₂O₅ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 681.0±55.0 °C(Predicted) | |
| Density: | 1.350±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected chiral building block, particularly in the preparation of complex peptides and peptidomimetics. Its structure includes a fluorenylmethyloxycarbonyl (Fmoc) group, which allows for orthogonal protection strategies in solid-phase peptide synthesis. The presence of both a piperidinone ring and a pyrrolidine scaffold makes it valuable for introducing conformational constraints into peptide chains, enhancing stability and selectivity. It is especially useful in the development of pharmaceutical intermediates, including protease inhibitors and other bioactive molecules where stereochemistry plays a critical role in activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $999.38 |
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| 0.100 | 10-20 days | $1,699.18 |
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(2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(2-oxopiperidin-1-yl)pyrrolidine-2-carboxylic acid
Widely used in peptide synthesis, this compound serves as a protected chiral building block, particularly in the preparation of complex peptides and peptidomimetics. Its structure includes a fluorenylmethyloxycarbonyl (Fmoc) group, which allows for orthogonal protection strategies in solid-phase peptide synthesis. The presence of both a piperidinone ring and a pyrrolidine scaffold makes it valuable for introducing conformational constraints into peptide chains, enhancing stability and selectivity. It is especially useful in the development of pharmaceutical intermediates, including protease inhibitors and other bioactive molecules where stereochemistry plays a critical role in activity.
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