tert-Butyl (1-benzyl-5-oxopyrrolidin-3-yl)carbamate
97%
- Product Code: 113094
CAS:
478832-03-0
| Molecular Weight: | 290.36 g./mol | Molecular Formula: | C₁₆H₂₂N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24393306 | |
| Melting Point: | Boiling Point: | 477.5±44.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals. It serves as an intermediate in the production of various biologically active molecules, including potential drug candidates. Its structure, featuring a pyrrolidinone ring and a benzyl group, makes it valuable for constructing complex molecules with therapeutic properties. It is often employed in peptide chemistry and medicinal chemistry research, where it aids in the synthesis of compounds targeting neurological disorders or other diseases. Additionally, its tert-butyl carbamate group acts as a protective group for amines, ensuring selective reactions during multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Powder Or Crystals |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $11.80 |
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| 0.250 | 10-20 days | $19.27 |
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| 1.000 | 10-20 days | $39.33 |
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tert-Butyl (1-benzyl-5-oxopyrrolidin-3-yl)carbamate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals. It serves as an intermediate in the production of various biologically active molecules, including potential drug candidates. Its structure, featuring a pyrrolidinone ring and a benzyl group, makes it valuable for constructing complex molecules with therapeutic properties. It is often employed in peptide chemistry and medicinal chemistry research, where it aids in the synthesis of compounds targeting neurological disorders or other diseases. Additionally, its tert-butyl carbamate group acts as a protective group for amines, ensuring selective reactions during multi-step synthetic processes.
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