(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-carbamoylphenyl)propanoic acid

≥95%

Reagent Code: #38027
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CAS Number 204716-17-6

science Other reagents with same CAS 204716-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.45 g/mol
Formula C₂₅H₂₂N₂O₅
badge Registry Numbers
MDL Number MFCD01317021
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality. The carbamoylphenyl moiety provides specific structural properties that can be tailored for targeted peptide sequences. It is particularly useful in the synthesis of bioactive peptides, pharmaceuticals, and research peptides, enabling precise control over the assembly of amino acids. The Fmoc group can be selectively removed under mild basic conditions, allowing for sequential peptide chain elongation without disrupting other functional groups. This makes it a valuable tool in the development of therapeutic peptides, enzyme inhibitors, and other biologically active molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿24,615.00
inventory 250mg
10-20 days ฿12,303.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-carbamoylphenyl)propanoic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality. The carbamoylphenyl moiety provides specific structural properties that can be tailored for targeted peptide sequences. It is particularly useful in the synthesis of bioactive peptides, pharmaceuticals, and research peptides, enabling precise

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality. The carbamoylphenyl moiety provides specific structural properties that can be tailored for targeted peptide sequences. It is particularly useful in the synthesis of bioactive peptides, pharmaceuticals, and research peptides, enabling precise control over the assembly of amino acids. The Fmoc group can be selectively removed under mild basic conditions, allowing for sequential peptide chain elongation without disrupting other functional groups. This makes it a valuable tool in the development of therapeutic peptides, enzyme inhibitors, and other biologically active molecules.

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