3-((Tert-butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
≥95%
- Product Code: 76244
CAS:
284493-52-3
| Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02090692 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the preparation of complex organic compounds, especially those involving peptide coupling reactions. The tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during synthesis. Its presence in the structure allows for controlled deprotection, which is crucial in multi-step synthetic processes. Additionally, the methoxyphenyl moiety can contribute to the compound's ability to interact with biological targets, making it valuable in drug discovery and medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,964.00 |
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| 0.250 | 10-20 days | ฿13,446.00 |
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| 1.000 | 10-20 days | ฿33,615.00 |
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3-((Tert-butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the preparation of complex organic compounds, especially those involving peptide coupling reactions. The tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during synthesis. Its presence in the structure allows for controlled deprotection, which is crucial in multi-step synthetic processes. Additionally, the methoxyphenyl moiety can contribute to the compound's ability to interact with biological targets, making it valuable in drug discovery and medicinal chemistry research.
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