Boc-(2S,4S)-4-amino-1-Fmoc-pyrrolidine-2-carboxylic Acid
≥95%
- Product Code: 50210
CAS:
221352-74-5
| Molecular Weight: | 452.50 g./mol | Molecular Formula: | C₂₅H₂₈N₂O₆ |
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| EC Number: | MDL Number: | MFCD02179641 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis, particularly in the construction of complex peptide chains. It serves as a protected amino acid derivative, allowing for selective deprotection and coupling during solid-phase peptide synthesis. The Boc (tert-butoxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups provide orthogonal protection, enabling precise control over the sequence of amino acids in the peptide. This compound is especially valuable in the synthesis of peptides with specific structural or functional requirements, such as those used in drug development, biochemical research, and the study of protein interactions. Its stability and compatibility with various synthetic protocols make it a versatile tool in organic and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £43.36 |
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| 0.250 | 10-20 days | £64.93 |
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| 1.000 | 10-20 days | £163.25 |
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| 5.000 | 10-20 days | £659.51 |
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Boc-(2S,4S)-4-amino-1-Fmoc-pyrrolidine-2-carboxylic Acid
This chemical is primarily used in peptide synthesis, particularly in the construction of complex peptide chains. It serves as a protected amino acid derivative, allowing for selective deprotection and coupling during solid-phase peptide synthesis. The Boc (tert-butoxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups provide orthogonal protection, enabling precise control over the sequence of amino acids in the peptide. This compound is especially valuable in the synthesis of peptides with specific structural or functional requirements, such as those used in drug development, biochemical research, and the study of protein interactions. Its stability and compatibility with various synthetic protocols make it a versatile tool in organic and medicinal chemistry.
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