(S)-3-(3-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid
98%
- Product Code: 54878
CAS:
500770-76-3
| Molecular Weight: | 344.2000 g./mol | Molecular Formula: | C₁₄H₁₈BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427924 | |
| Melting Point: | Boiling Point: | 471.1 °C at 760 mmHg | |
| Density: | 1.403g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, including those related to dopamine regulation. Its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable for constructing complex molecules with specific biological activities.
In medicinal chemistry, it is often employed in peptide coupling reactions and as a building block for creating chiral molecules, which are crucial for designing enantiomerically pure drugs. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, enabling precise control over the final product's structure. Additionally, its bromine substituent allows for further functionalization through cross-coupling reactions, expanding its utility in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,601.00 |
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(S)-3-(3-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, including those related to dopamine regulation. Its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable for constructing complex molecules with specific biological activities.
In medicinal chemistry, it is often employed in peptide coupling reactions and as a building block for creating chiral molecules, which are crucial for designing enantiomerically pure drugs. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, enabling precise control over the final product's structure. Additionally, its bromine substituent allows for further functionalization through cross-coupling reactions, expanding its utility in drug discovery and development.
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