(3R,4S)-1-((Benzyloxy)carbonyl)-4-fluoropyrrolidine-3-carboxylic acid
98%
- Product Code: 36750
CAS:
1269755-11-4
| Molecular Weight: | 267.2600 g./mol | Molecular Formula: | C₁₃H₁₄FNO₄ |
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| EC Number: | MDL Number: | MFCD22573909 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated pyrrolidine ring and a benzyloxycarbonyl protecting group, makes it valuable in the development of biologically active compounds, particularly in the creation of peptide-based drugs and enzyme inhibitors. The presence of fluorine enhances the metabolic stability and binding affinity of the resulting molecules, making it useful in designing drugs targeting neurological disorders, cancer, and other diseases. Additionally, it serves as a building block in organic synthesis for constructing chiral centers, which are crucial for producing enantiomerically pure pharmaceuticals. Its applications are also explored in medicinal chemistry for optimizing drug candidates with improved efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿14,067.00 |
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(3R,4S)-1-((Benzyloxy)carbonyl)-4-fluoropyrrolidine-3-carboxylic acid
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated pyrrolidine ring and a benzyloxycarbonyl protecting group, makes it valuable in the development of biologically active compounds, particularly in the creation of peptide-based drugs and enzyme inhibitors. The presence of fluorine enhances the metabolic stability and binding affinity of the resulting molecules, making it useful in designing drugs targeting neurological disorders, cancer, and other diseases. Additionally, it serves as a building block in organic synthesis for constructing chiral centers, which are crucial for producing enantiomerically pure pharmaceuticals. Its applications are also explored in medicinal chemistry for optimizing drug candidates with improved efficacy and reduced side effects.
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