(S)-methyl 3-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)propanoate
95%
- Product Code: 83003
CAS:
277745-41-2
| Molecular Weight: | 297.32 g./mol | Molecular Formula: | C₁₅H₂₀FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 401.9±40.0 °C(Predicted) | |
| Density: | 1.149±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules, particularly those with potential therapeutic applications. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of drugs targeting neurological disorders, cancer, and other diseases. The fluorine atom enhances the bioavailability and metabolic stability of the resulting drug candidates, while the Boc group allows for selective deprotection during synthesis. It is often employed in peptide coupling reactions and as a building block for chiral compounds, contributing to the creation of enantiomerically pure drugs. Its applications are critical in medicinal chemistry research, where it aids in the discovery and optimization of new drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,360.00 |
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| 0.250 | 10-20 days | ฿17,550.00 |
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| 1.000 | 10-20 days | ฿35,100.00 |
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(S)-methyl 3-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)propanoate
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules, particularly those with potential therapeutic applications. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of drugs targeting neurological disorders, cancer, and other diseases. The fluorine atom enhances the bioavailability and metabolic stability of the resulting drug candidates, while the Boc group allows for selective deprotection during synthesis. It is often employed in peptide coupling reactions and as a building block for chiral compounds, contributing to the creation of enantiomerically pure drugs. Its applications are critical in medicinal chemistry research, where it aids in the discovery and optimization of new drug candidates.
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