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

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Reagent Code: #38026
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CAS Number 178432-48-9

science Other reagents with same CAS 178432-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.43 g/mol
Formula C₂₄H₂₁NO₅
badge Registry Numbers
MDL Number MFCD07371961
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. It is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. The hydroxyl group on the phenyl ring can also participate in further functionalization or interactions, making it useful in designing peptides with specific biological activities. Its application is common in pharmaceutical research, drug development, and biochemical studies involving peptide-based therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,275.00
inventory 250mg
10-20 days ฿8,550.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. It is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. The hydroxyl group on the phenyl ring can also participate in further functionalization or interaction

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. It is particularly valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. The hydroxyl group on the phenyl ring can also participate in further functionalization or interactions, making it useful in designing peptides with specific biological activities. Its application is common in pharmaceutical research, drug development, and biochemical studies involving peptide-based therapeutics.

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