Methyl 2-((tert-butoxycarbonyl)amino)-2-phenylacetate
95%
- Product Code: 58536
CAS:
169512-94-1
| Molecular Weight: | 265.30 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458977 | |
| Melting Point: | 133-135 °C | Boiling Point: | 383.7±35.0 °C(Predicted) |
| Density: | 1.115±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of peptides and other biologically active molecules. The tert-butoxycarbonyl (Boc) group protects the amino functionality during chemical reactions, allowing selective modifications to the ester group or other parts of the molecule. It is particularly valuable in medicinal chemistry for the development of pharmaceutical compounds, including drugs targeting neurological and metabolic disorders. Additionally, it finds application in the synthesis of chiral compounds, leveraging its phenyl group for stereochemical control in asymmetric synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £116.43 |
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| 0.250 | 10-20 days | £230.01 |
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| 1.000 | 10-20 days | £574.43 |
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Methyl 2-((tert-butoxycarbonyl)amino)-2-phenylacetate
This compound is primarily used in organic synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of peptides and other biologically active molecules. The tert-butoxycarbonyl (Boc) group protects the amino functionality during chemical reactions, allowing selective modifications to the ester group or other parts of the molecule. It is particularly valuable in medicinal chemistry for the development of pharmaceutical compounds, including drugs targeting neurological and metabolic disorders. Additionally, it finds application in the synthesis of chiral compounds, leveraging its phenyl group for stereochemical control in asymmetric synthesis.
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