(S)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-6-aminohexanoate hydrochloride
97%
- Product Code: 104348
CAS:
2413365-23-6
| Molecular Weight: | 460.99 g./mol | Molecular Formula: | C₂₅H₃₃ClN₂O₄ |
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| EC Number: | MDL Number: | MFCD32066818 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The tert-butyl ester protects the carboxylic acid group, ensuring it remains inert until the final deprotection step. This chemical is particularly valuable in synthesizing peptides with specific sequences, as it provides control over the introduction of amino acids at desired positions. Its application is crucial in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise peptide structures are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $55.15 |
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| 0.250 | 10-20 days | $92.21 |
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(S)-tert-Butyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-6-aminohexanoate hydrochloride
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a temporary protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The tert-butyl ester protects the carboxylic acid group, ensuring it remains inert until the final deprotection step. This chemical is particularly valuable in synthesizing peptides with specific sequences, as it provides control over the introduction of amino acids at desired positions. Its application is crucial in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise peptide structures are required.
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