(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid

95%

Reagent Code: #57127
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CAS Number 84030-19-3

science Other reagents with same CAS 84030-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 467.52 g/mol
Formula C₂₈H₂₅N₃O₄
badge Registry Numbers
MDL Number MFCD00038537
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain elongation. The benzyl-protected imidazole moiety allows for the incorporation of histidine-like structures into peptides, which is valuable for studying enzyme active sites, protein-protein interactions, and designing bioactive peptides. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs, including antimicrobial agents, hormone analogs, and enzyme inhibitors. Additionally, it is used in biochemical studies to investigate the role of histidine residues in protein function and stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿900.00
1g
10-20 days ฿2,340.00
5g
10-20 days ฿8,190.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain elongation. The benzyl-protected imidazole moiety allows for the incorporation of histidine-like structures into peptides, which is val

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain elongation. The benzyl-protected imidazole moiety allows for the incorporation of histidine-like structures into peptides, which is valuable for studying enzyme active sites, protein-protein interactions, and designing bioactive peptides. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs, including antimicrobial agents, hormone analogs, and enzyme inhibitors. Additionally, it is used in biochemical studies to investigate the role of histidine residues in protein function and stability.

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