(1S,2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid
≥95%
- Product Code: 36250
CAS:
359586-64-4
Molecular Weight: | 351.40 g./mol | Molecular Formula: | C₂₁H₂₁NO₄ |
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EC Number: | MDL Number: | MFCD04112694 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
(1S,2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid is primarily used in peptide synthesis. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethoxycarbonyl) group acts as a protecting group for the amine functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of peptides. The compound is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and protection of amino acids is critical. Its application is common in pharmaceutical research, biotechnology, and the development of therapeutic peptides.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white powder or crystals |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿7,550.00 |
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(1S,2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid
(1S,2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid is primarily used in peptide synthesis. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethoxycarbonyl) group acts as a protecting group for the amine functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of peptides. The compound is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and protection of amino acids is critical. Its application is common in pharmaceutical research, biotechnology, and the development of therapeutic peptides.
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