(S)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride
≥95%
- Product Code: 38157
CAS:
1217828-88-0
| Molecular Weight: | 189.64 g./mol | Molecular Formula: | C₈H₁₂ClNO₂ |
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| EC Number: | MDL Number: | MFCD06659383 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrrolidine ring and a propargyl group, makes it a valuable building block for developing potential drug candidates, particularly those targeting neurological disorders. The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is crucial in designing drugs with high specificity and reduced side effects. Additionally, it has been explored in the development of inhibitors for enzymes involved in disease pathways, such as those related to inflammation or cancer. Its applications extend to research in peptide chemistry, where it can be incorporated into peptide chains to modify their biological activity or stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $486.59 |
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| 0.250 | 10-20 days | $973.18 |
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(S)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrrolidine ring and a propargyl group, makes it a valuable building block for developing potential drug candidates, particularly those targeting neurological disorders. The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is crucial in designing drugs with high specificity and reduced side effects. Additionally, it has been explored in the development of inhibitors for enzymes involved in disease pathways, such as those related to inflammation or cancer. Its applications extend to research in peptide chemistry, where it can be incorporated into peptide chains to modify their biological activity or stability.
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