(2S,3S)-3-Hydroxypyrrolidine-2-carboxylic acid
97%
- Product Code: 38478
CAS:
4298-08-2
Molecular Weight: | 131.13 g./mol | Molecular Formula: | C₅H₉NO₃ |
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EC Number: | MDL Number: | MFCD00216471 | |
Melting Point: | Boiling Point: | 355.2°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly as a chiral building block in the production of drugs targeting neurological and metabolic disorders. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it serves as an intermediate in the development of protease inhibitors, which are used in treatments for conditions like HIV and hepatitis. Its role in peptide synthesis also extends to research applications, where it aids in studying protein interactions and enzyme mechanisms.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | Off white to Pale-yellow to Yellow-brown Solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,790.00 |
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0.250 | 10-20 days | ฿10,290.00 |
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1.000 | 10-20 days | ฿25,740.00 |
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(2S,3S)-3-Hydroxypyrrolidine-2-carboxylic acid
This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly as a chiral building block in the production of drugs targeting neurological and metabolic disorders. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it serves as an intermediate in the development of protease inhibitors, which are used in treatments for conditions like HIV and hepatitis. Its role in peptide synthesis also extends to research applications, where it aids in studying protein interactions and enzyme mechanisms.
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