(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-carbamoylphenyl)propanoic acid

97%

  • Product Code: 104325
  CAS:    959573-22-9
Molecular Weight: 430.45 g./mol Molecular Formula: C₂₅H₂₂N₂O₅
EC Number: MDL Number: MFCD06659144
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which can be selectively removed under mild basic conditions. The carbamoylphenyl side chain makes it suitable for incorporating specific functional groups into peptides, enhancing their biological activity or binding properties. It is often employed in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and signaling pathways. Its stability and compatibility with various synthesis protocols make it a versatile building block in organic and medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days Ft11,442.10
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-
0.250 10-20 days Ft28,120.42
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1.000 10-20 days Ft68,846.55
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-carbamoylphenyl)propanoic acid
This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which can be selectively removed under mild basic conditions. The carbamoylphenyl side chain makes it suitable for incorporating specific functional groups into peptides, enhancing their biological activity or binding properties. It is often employed in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and signaling pathways. Its stability and compatibility with various synthesis protocols make it a versatile building block in organic and medicinal chemistry.
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