(3S,4R)-1-(Tert-butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid
95%
- Product Code: 76156
CAS:
884048-45-7
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD06796141 | |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex molecules, particularly in the development of drugs targeting neurological disorders. Its chiral structure makes it valuable for creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in peptide synthesis, where it serves as a building block for constructing specific peptide sequences with desired biological activities. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its utility in organic chemistry research and drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,193.00 |
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| 0.250 | 10-20 days | ฿8,307.00 |
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| 1.000 | 10-20 days | ฿20,835.00 |
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(3S,4R)-1-(Tert-butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex molecules, particularly in the development of drugs targeting neurological disorders. Its chiral structure makes it valuable for creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in peptide synthesis, where it serves as a building block for constructing specific peptide sequences with desired biological activities. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its utility in organic chemistry research and drug development.
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