(2S,3R)-1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-2-carboxylic acid
98%
- Product Code: 76138
CAS:
186132-96-7
| Molecular Weight: | 231.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458682 | |
| Melting Point: | Boiling Point: | 390.87 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting central nervous system disorders. Its chiral structure makes it valuable for producing enantiomerically pure active pharmaceutical ingredients (APIs), ensuring higher efficacy and reduced side effects. It is also employed in the development of peptide-based therapeutics, where it serves as a building block for constructing complex peptide chains. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it a versatile tool in organic chemistry. Researchers also utilize it in the study of enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,905.00 |
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| 0.100 | 10-20 days | ฿7,353.00 |
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| 0.250 | 10-20 days | ฿11,754.00 |
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(2S,3R)-1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-2-carboxylic acid
This compound is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting central nervous system disorders. Its chiral structure makes it valuable for producing enantiomerically pure active pharmaceutical ingredients (APIs), ensuring higher efficacy and reduced side effects. It is also employed in the development of peptide-based therapeutics, where it serves as a building block for constructing complex peptide chains. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it a versatile tool in organic chemistry. Researchers also utilize it in the study of enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
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