L-Aspartic acid 1-benzyl ester
98%
- Product Code: 105274
Alias:
L-Aspartate 1-Benzyl Ester
CAS:
7362-93-8
| Molecular Weight: | 223.2 g./mol | Molecular Formula: | C₁₁H₁₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063186 | |
| Melting Point: | 176 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
L-Aspartic acid 1-benzyl ester is widely used in organic synthesis, particularly in peptide chemistry. It serves as a key intermediate for the preparation of peptides and amino acid derivatives. The benzyl ester group acts as a protecting group for the carboxyl function, allowing selective reactions to occur at other sites of the molecule. This compound is especially valuable in the synthesis of complex peptides, where controlled deprotection and coupling steps are essential. Additionally, it finds applications in the development of pharmaceuticals and bioactive compounds, where precise structural modifications are required. Its role in facilitating the synthesis of tailored amino acid derivatives makes it a crucial component in medicinal chemistry and biochemical research.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White To Very Pale Yellow Powder Or Crystals |
| Purity (%) | 97.5-100 |
| Specific Rotation [A]20/D(C=1,0.1M HCL) | -17.0 to -12.0 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $15.37 |
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| 5.000 | 10-20 days | $46.51 |
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| 25.000 | 10-20 days | $177.74 |
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L-Aspartic acid 1-benzyl ester
L-Aspartic acid 1-benzyl ester is widely used in organic synthesis, particularly in peptide chemistry. It serves as a key intermediate for the preparation of peptides and amino acid derivatives. The benzyl ester group acts as a protecting group for the carboxyl function, allowing selective reactions to occur at other sites of the molecule. This compound is especially valuable in the synthesis of complex peptides, where controlled deprotection and coupling steps are essential. Additionally, it finds applications in the development of pharmaceuticals and bioactive compounds, where precise structural modifications are required. Its role in facilitating the synthesis of tailored amino acid derivatives makes it a crucial component in medicinal chemistry and biochemical research.
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