(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
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
0.100 10-20 days £58.62
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0.250 10-20 days £97.71
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1.000 10-20 days £219.84
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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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