(S)-3-(3-Aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
98%
- Product Code: 113770
CAS:
170157-55-8
| Molecular Weight: | 280.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19441578 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of peptide-based drugs, where its structure allows for the incorporation of specific amino acid sequences. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for selective reactions during peptide synthesis, ensuring that the amine group remains protected until the desired stage of the process. Additionally, its chiral center enables the creation of enantiomerically pure compounds, which is essential for drugs targeting specific biological pathways. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for therapeutic purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,033.00 |
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| 0.250 | 10-20 days | ฿18,018.00 |
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| 1.000 | 10-20 days | ฿45,018.00 |
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(S)-3-(3-Aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
This chemical is primarily used in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of peptide-based drugs, where its structure allows for the incorporation of specific amino acid sequences. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for selective reactions during peptide synthesis, ensuring that the amine group remains protected until the desired stage of the process. Additionally, its chiral center enables the creation of enantiomerically pure compounds, which is essential for drugs targeting specific biological pathways. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for therapeutic purposes.
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