(4S,5R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)-L-isoleucyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid
98%
- Product Code: 235918
CAS:
957780-52-8
| Molecular Weight: | 494.58 g./mol | Molecular Formula: | C₂₈H₃₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18427359 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the preparation of enantiomerically pure peptides and complex organic molecules. Its structure supports stereochemical control during bond formation, making it valuable in pharmaceutical research for developing optically active drugs. Commonly employed in solid-phase peptide synthesis (SPPS) due to the Fmoc group, which allows for mild base-induced deprotection while maintaining stability under various reaction conditions. The oxazolidine ring enhances conformational rigidity, improving selectivity in transformations such as alkylations, acylations, and nucleophilic additions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿6,010.00 |
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(4S,5R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)-L-isoleucyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid
Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the preparation of enantiomerically pure peptides and complex organic molecules. Its structure supports stereochemical control during bond formation, making it valuable in pharmaceutical research for developing optically active drugs. Commonly employed in solid-phase peptide synthesis (SPPS) due to the Fmoc group, which allows for mild base-induced deprotection while maintaining stability under various reaction conditions. The oxazolidine ring enhances conformational rigidity, improving selectivity in transformations such as alkylations, acylations, and nucleophilic additions.
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