D-Leucine benzyl ester p-toluenesulfonate
98%
- Product Code: 67144
Alias:
D-Leucine Benzyl Ester p-Toluenesulfonate
CAS:
17664-93-6
| Molecular Weight: | 393.5 g./mol | Molecular Formula: | C₁₃H₁₉NO₂C₇H₈O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066116 | |
| Melting Point: | 158 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
D-Leucine benzyl ester p-toluenesulfonate is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of peptides and other bioactive compounds. The benzyl ester group provides protection for carboxylic acids during synthetic processes, ensuring selective reactions. This compound is particularly valuable in the development of enantiomerically pure substances, contributing to the study of chiral molecules in drug design. Its application extends to the synthesis of amino acid derivatives, which are essential in creating therapeutic agents and studying biochemical pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $24.11 |
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| 5.000 | 10-20 days | $40.18 |
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D-Leucine benzyl ester p-toluenesulfonate
D-Leucine benzyl ester p-toluenesulfonate is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of peptides and other bioactive compounds. The benzyl ester group provides protection for carboxylic acids during synthetic processes, ensuring selective reactions. This compound is particularly valuable in the development of enantiomerically pure substances, contributing to the study of chiral molecules in drug design. Its application extends to the synthesis of amino acid derivatives, which are essential in creating therapeutic agents and studying biochemical pathways.
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