(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(o-tolyl)propanoic acid
98%
- Product Code: 104978
CAS:
501015-26-5
Molecular Weight: | 401.45 g./mol | Molecular Formula: | C₂₅H₂₃NO₄ |
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EC Number: | MDL Number: | MFCD03427971 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality during the synthesis process. This allows for selective deprotection and coupling reactions, enabling the step-by-step assembly of peptides. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. The compound's specific structure, including the o-tolyl group, can influence the properties of the resulting peptides, such as stability, binding affinity, or biological activity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,592.00 |
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0.250 | 10-20 days | ฿4,320.00 |
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1.000 | 10-20 days | ฿9,720.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(o-tolyl)propanoic acid
This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality during the synthesis process. This allows for selective deprotection and coupling reactions, enabling the step-by-step assembly of peptides. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. The compound's specific structure, including the o-tolyl group, can influence the properties of the resulting peptides, such as stability, binding affinity, or biological activity.
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