4-tert-Butyl N-[(tert-butoxy)carbonyl]-L-aspartate dicyclohexylamine salt
98%
- Product Code: 66116
Alias:
N-tert-butoxycarbonyl-L-aspartic acid 4-tert-butyl ester dicyclohexylamine salt
CAS:
1913-12-8
| Molecular Weight: | 470.64 g./mol | Molecular Formula: | C₁₃H₂₃NO₆C₁₂H₂₃N |
|---|---|---|---|
| EC Number: | 217-626-7 | MDL Number: | MFCD00038889 |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized in the synthesis of peptides and amino acid derivatives. It serves as a protected form of L-aspartic acid, enabling controlled reactions in peptide bond formation without unwanted side reactions. The tert-butyl and tert-butoxycarbonyl (Boc) groups act as protective groups, which can be selectively removed under mild acidic conditions, allowing for further modifications or elongation of the peptide chain. Its dicyclohexylamine salt form enhances stability and solubility, making it suitable for use in organic synthesis and pharmaceutical research. This compound is particularly valuable in the production of complex peptides, including those with therapeutic applications, such as hormone analogs or enzyme inhibitors.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 98-100 |
| SPECIFIC ROTATION A20DC1 IN ETOH | 17-21 |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| TLC ANALYSIS | ONE SPOT |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,770.94 |
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| 5.000 | 10-20 days | Ft11,205.07 |
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| 25.000 | 10-20 days | Ft38,786.79 |
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4-tert-Butyl N-[(tert-butoxy)carbonyl]-L-aspartate dicyclohexylamine salt
This chemical is primarily utilized in the synthesis of peptides and amino acid derivatives. It serves as a protected form of L-aspartic acid, enabling controlled reactions in peptide bond formation without unwanted side reactions. The tert-butyl and tert-butoxycarbonyl (Boc) groups act as protective groups, which can be selectively removed under mild acidic conditions, allowing for further modifications or elongation of the peptide chain. Its dicyclohexylamine salt form enhances stability and solubility, making it suitable for use in organic synthesis and pharmaceutical research. This compound is particularly valuable in the production of complex peptides, including those with therapeutic applications, such as hormone analogs or enzyme inhibitors.
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