(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)hexanoate
98%
- Product Code: 60742
CAS:
133628-28-1
Molecular Weight: | 482.57 g./mol | Molecular Formula: | C₂₇H₃₄N₂O₆ |
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EC Number: | MDL Number: | MFCD00236856 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, enabling the controlled construction of peptide chains. The fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as protective groups for the amino functionalities, preventing unwanted reactions during synthesis. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures precise and sequential addition of amino acids. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, allowing for the creation of complex peptides with high purity and specificity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,143.00 |
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1.000 | 10-20 days | ฿2,205.00 |
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5.000 | 10-20 days | ฿10,980.00 |
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(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)hexanoate
This chemical is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, enabling the controlled construction of peptide chains. The fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as protective groups for the amino functionalities, preventing unwanted reactions during synthesis. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures precise and sequential addition of amino acids. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, allowing for the creation of complex peptides with high purity and specificity.
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