(S)-3-Methyl-pyrrolidine-3-carboxylic acid
97%
- Product Code: 38473
CAS:
1427203-57-3
| Molecular Weight: | 129.1570 g./mol | Molecular Formula: | C₆H₁₁NO₂ |
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| EC Number: | MDL Number: | MFCD24368649 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(S)-3-Methyl-pyrrolidine-3-carboxylic acid is primarily utilized as a chiral building block in the synthesis of various pharmaceutical compounds. Its stereochemistry makes it valuable in the development of drugs that require specific enantiomeric forms for enhanced efficacy and reduced side effects. It is often employed in the production of active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders, such as Parkinson’s disease, due to its structural similarity to neurotransmitters. Additionally, it serves as a key intermediate in the synthesis of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor modulators. Its application extends to the development of peptidomimetics, where it contributes to the stability and bioavailability of peptide-based drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,687.00 |
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(S)-3-Methyl-pyrrolidine-3-carboxylic acid
(S)-3-Methyl-pyrrolidine-3-carboxylic acid is primarily utilized as a chiral building block in the synthesis of various pharmaceutical compounds. Its stereochemistry makes it valuable in the development of drugs that require specific enantiomeric forms for enhanced efficacy and reduced side effects. It is often employed in the production of active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders, such as Parkinson’s disease, due to its structural similarity to neurotransmitters. Additionally, it serves as a key intermediate in the synthesis of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor modulators. Its application extends to the development of peptidomimetics, where it contributes to the stability and bioavailability of peptide-based drugs.
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