(2S,4R)-1-(tert-Butoxycarbonyl)-4-(3-chlorobenzyl)pyrrolidine-2-carboxylic acid
≥95%
- Product Code: 86421
CAS:
959576-36-4
| Molecular Weight: | 339.81 g./mol | Molecular Formula: | C₁₇H₂₂ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659395 | |
| Melting Point: | Boiling Point: | 472.4±35.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research fields. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a pyrrolidine ring and a chlorobenzyl group, makes it a valuable building block for creating compounds with potential therapeutic effects. Researchers often employ it in the preparation of peptide analogs and enzyme inhibitors, where its stereochemistry and functional groups play a critical role in enhancing binding affinity and selectivity. Additionally, it is used in medicinal chemistry studies to explore structure-activity relationships and optimize drug candidates for improved efficacy and safety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,180.00 |
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(2S,4R)-1-(tert-Butoxycarbonyl)-4-(3-chlorobenzyl)pyrrolidine-2-carboxylic acid
This compound is primarily utilized in the pharmaceutical and chemical research fields. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a pyrrolidine ring and a chlorobenzyl group, makes it a valuable building block for creating compounds with potential therapeutic effects. Researchers often employ it in the preparation of peptide analogs and enzyme inhibitors, where its stereochemistry and functional groups play a critical role in enhancing binding affinity and selectivity. Additionally, it is used in medicinal chemistry studies to explore structure-activity relationships and optimize drug candidates for improved efficacy and safety.
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