(R)-5-(Pyrrolidin-2-yl)-1H-tetrazole
95%
- Product Code: 113582
CAS:
702700-79-6
| Molecular Weight: | 139.16 g./mol | Molecular Formula: | C₅H₉N₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19228007 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a pyrrolidine ring and a tetrazole moiety, makes it a valuable scaffold for designing drugs with potential therapeutic effects. Specifically, it has been explored in the development of enzyme inhibitors, particularly those targeting proteases and kinases, which are crucial in treating diseases like cancer, viral infections, and inflammatory disorders. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of potential drug candidates. Researchers also investigate its use in peptidomimetics, where it serves as a mimic of peptide bonds, improving the stability and bioavailability of peptide-based drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,456.00 |
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| 1.000 | 10-20 days | ฿5,274.00 |
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| 5.000 | 10-20 days | ฿15,822.00 |
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(R)-5-(Pyrrolidin-2-yl)-1H-tetrazole
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a pyrrolidine ring and a tetrazole moiety, makes it a valuable scaffold for designing drugs with potential therapeutic effects. Specifically, it has been explored in the development of enzyme inhibitors, particularly those targeting proteases and kinases, which are crucial in treating diseases like cancer, viral infections, and inflammatory disorders. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of potential drug candidates. Researchers also investigate its use in peptidomimetics, where it serves as a mimic of peptide bonds, improving the stability and bioavailability of peptide-based drugs.
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