(S)-tert-Butyl (1-(1,3-dioxoisoindolin-2-yl)-3-(3-fluorophenyl)propan-2-yl)carbamate
97%
- Product Code: 113611
CAS:
1201923-48-9
| Molecular Weight: | 398.43 g./mol | Molecular Formula: | C₂₂H₂₃FN₂O₄ |
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| EC Number: | MDL Number: | MFCD28359281 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorophenyl group and a dioxoisoindoline moiety, makes it a valuable building block for developing potential pharmaceuticals, particularly in the design of enzyme inhibitors or receptor modulators. The presence of the tert-butyl carbamate group provides stability and facilitates further chemical modifications, enabling the creation of targeted drug candidates. Researchers often employ it in the development of compounds for treating neurological disorders or cancer, where selective interaction with biological targets is crucial. Its application is also seen in peptide chemistry, where it serves as a protective group during the synthesis of complex peptide structures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft16,775.29 |
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| 0.250 | 10-20 days | Ft28,411.32 |
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(S)-tert-Butyl (1-(1,3-dioxoisoindolin-2-yl)-3-(3-fluorophenyl)propan-2-yl)carbamate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorophenyl group and a dioxoisoindoline moiety, makes it a valuable building block for developing potential pharmaceuticals, particularly in the design of enzyme inhibitors or receptor modulators. The presence of the tert-butyl carbamate group provides stability and facilitates further chemical modifications, enabling the creation of targeted drug candidates. Researchers often employ it in the development of compounds for treating neurological disorders or cancer, where selective interaction with biological targets is crucial. Its application is also seen in peptide chemistry, where it serves as a protective group during the synthesis of complex peptide structures.
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