N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartic Acid
≥98.0%(HPLC)
- Product Code: 77646
CAS:
136083-57-3
| Molecular Weight: | 355.35 g./mol | Molecular Formula: | C₁₉H₁₇NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318740 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used extensively in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), it serves as a protected form of aspartic acid. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, preventing unwanted reactions. This allows for the selective deprotection and coupling of amino acids, ensuring the accurate assembly of peptide chains. It is especially valuable in the production of complex peptides and proteins for pharmaceutical research and development. The compound’s stability and ease of removal under mild conditions make it a preferred choice in peptide chemistry. Additionally, it is utilized in the synthesis of bioactive peptides, which have applications in drug discovery and therapeutic treatments.
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 | ฿770.00 |
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| 5.000 | 10-20 days | ฿2,820.00 |
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| 25.000 | 10-20 days | ฿6,290.00 |
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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartic Acid
Used extensively in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), it serves as a protected form of aspartic acid. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, preventing unwanted reactions. This allows for the selective deprotection and coupling of amino acids, ensuring the accurate assembly of peptide chains. It is especially valuable in the production of complex peptides and proteins for pharmaceutical research and development. The compound’s stability and ease of removal under mild conditions make it a preferred choice in peptide chemistry. Additionally, it is utilized in the synthesis of bioactive peptides, which have applications in drug discovery and therapeutic treatments.
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