(S)-5-((Trityloxy)methyl)pyrrolidin-2-one
97%
- Product Code: 82112
CAS:
105526-85-0
| Molecular Weight: | 357.44 g./mol | Molecular Formula: | C₂₄H₂₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075592 | |
| Melting Point: | 164-166 °C | Boiling Point: | 533.0±45.0 °C(Predicted) |
| Density: | 1.142±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of various bioactive molecules, including antiviral and anticancer agents. Its structure, featuring a trityl-protected hydroxyl group, allows for selective deprotection and further functionalization, making it valuable in complex multi-step synthesis processes. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving the desired enantiomeric purity. Researchers also leverage its stability and reactivity in the design of novel drug candidates, particularly in the development of prodrugs and targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $274.34 |
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| 1.000 | 10-20 days | $333.02 |
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| 5.000 | 10-20 days | $1,176.60 |
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(S)-5-((Trityloxy)methyl)pyrrolidin-2-one
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of various bioactive molecules, including antiviral and anticancer agents. Its structure, featuring a trityl-protected hydroxyl group, allows for selective deprotection and further functionalization, making it valuable in complex multi-step synthesis processes. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving the desired enantiomeric purity. Researchers also leverage its stability and reactivity in the design of novel drug candidates, particularly in the development of prodrugs and targeted therapies.
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