(2S,4R)-4-Fluoro-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester
≥98%,≥99% e.e.
- Product Code: 70891
CAS:
203866-14-2
Molecular Weight: | 233.2 g./mol | Molecular Formula: | C₁₀H₁₆FNO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 346.0±42.0 °C | |
Density: | 1.24±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its unique stereochemistry and functional groups make it valuable for constructing complex drug candidates, particularly in the development of protease inhibitors and other enzyme-targeting therapeutics. The fluorine atom enhances the molecule's stability and binding affinity, while the tert-butyl ester group provides protection during synthetic processes, ensuring selective reactions. It is often employed in the production of antiviral and anticancer agents, contributing to the creation of more effective and targeted treatments.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White to Off-white to Tan Powder or Crystals |
PURITY | 97.5-100 |
OPTICAL PURITYEE | 98.5 100% |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿500.00 |
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5.000 | 10-20 days | ฿1,890.00 |
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10.000 | 10-20 days | ฿3,270.00 |
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25.000 | 10-20 days | ฿7,690.00 |
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(2S,4R)-4-Fluoro-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its unique stereochemistry and functional groups make it valuable for constructing complex drug candidates, particularly in the development of protease inhibitors and other enzyme-targeting therapeutics. The fluorine atom enhances the molecule's stability and binding affinity, while the tert-butyl ester group provides protection during synthetic processes, ensuring selective reactions. It is often employed in the production of antiviral and anticancer agents, contributing to the creation of more effective and targeted treatments.
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