Boc-D-Asp(OcHex)-OH
98%
- Product Code: 105731
Alias:
tert-butoxycarbonyl D-aspartic acid β-cyclohexyl ester
CAS:
112898-18-7
| Molecular Weight: | 315.36 g./mol | Molecular Formula: | C₁₅H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00060741 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in peptide synthesis, this compound serves as a protected form of D-aspartic acid. The Boc (tert-butoxycarbonyl) group safeguards the amino functionality, while the OcHex (cyclohexyl ester) group protects the carboxyl group during the synthesis process. This protection is crucial to prevent unwanted side reactions and ensure the correct sequence of amino acids in the final peptide product. It is particularly valuable in the production of complex peptides and proteins, where precise control over the assembly of amino acids is essential. Additionally, its application extends to the development of pharmaceuticals, where modified peptides are often used as active ingredients or intermediates in drug synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Appearance | White To Off-White Powder Or Solid Or Chunks |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €29.02 |
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| 5.000 | 10-20 days | €91.81 |
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| 25.000 | 10-20 days | €311.31 |
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Boc-D-Asp(OcHex)-OH
Used primarily in peptide synthesis, this compound serves as a protected form of D-aspartic acid. The Boc (tert-butoxycarbonyl) group safeguards the amino functionality, while the OcHex (cyclohexyl ester) group protects the carboxyl group during the synthesis process. This protection is crucial to prevent unwanted side reactions and ensure the correct sequence of amino acids in the final peptide product. It is particularly valuable in the production of complex peptides and proteins, where precise control over the assembly of amino acids is essential. Additionally, its application extends to the development of pharmaceuticals, where modified peptides are often used as active ingredients or intermediates in drug synthesis.
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