(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid
95%
- Product Code: 113672
CAS:
1821775-99-8
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in the preparation of protease inhibitors, which are crucial in treating diseases such as HIV/AIDS and hepatitis C. Additionally, it serves as a building block in the synthesis of complex molecules for neurological and cardiovascular drugs, where precise stereochemistry is critical for efficacy. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile reagent in multi-step organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft150,880.61 |
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| 1.000 | 10-20 days | Ft361,686.81 |
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(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid
(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in the preparation of protease inhibitors, which are crucial in treating diseases such as HIV/AIDS and hepatitis C. Additionally, it serves as a building block in the synthesis of complex molecules for neurological and cardiovascular drugs, where precise stereochemistry is critical for efficacy. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile reagent in multi-step organic synthesis.
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