(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromopyridin-2-yl)propanoic acid

95%

Reagent Code: #38028
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CAS Number 282734-37-6

science Other reagents with same CAS 282734-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 467.31 g/mol
Formula C₂₃H₁₉BrN₂O₄
badge Registry Numbers
MDL Number MFCD11615774
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromopyridinyl moiety can act as a reactive handle for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, bioconjugates, or probes. Its application is particularly relevant in medicinal chemistry and biochemical research, where precise control over peptide sequences and modifications is essential. Additionally, the bromine atom can facilitate cross-coupling reactions, enabling the introduction of diverse chemical groups for advanced structural modifications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿16,960.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromopyridin-2-yl)propanoic acid
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This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromopyridinyl moiety can act as a reactive handle for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, bioconjugates, or probes. Its application is particularly relevant in medicinal c

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromopyridinyl moiety can act as a reactive handle for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, bioconjugates, or probes. Its application is particularly relevant in medicinal chemistry and biochemical research, where precise control over peptide sequences and modifications is essential. Additionally, the bromine atom can facilitate cross-coupling reactions, enabling the introduction of diverse chemical groups for advanced structural modifications.

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