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

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Reagent Code: #38030
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CAS Number 158171-15-4

science Other reagents with same CAS 158171-15-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 407.3100 g/mol
Formula C₁₈H₁₈NO₈P
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Storage room temperature

description Product Description

This chemical is primarily utilized in the field of peptide synthesis, where it serves as a crucial building block for the incorporation of phosphoserine residues into peptides. Its Fmoc-protected amino acid structure allows for selective deprotection during solid-phase peptide synthesis, enabling the precise construction of phosphopeptides. These phosphopeptides are essential tools in biochemical research, particularly in studying protein phosphorylation, signal transduction pathways, and enzyme-substrate interactions. Additionally, the compound is employed in the development of peptide-based drugs and diagnostics, where phosphorylation plays a critical role in modulating biological activity. Its application extends to the preparation of affinity ligands for purifying phosphorylated proteins and antibodies, aiding in proteomics and immunology studies.

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Test Parameter Specification
Appearance solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 100mg
10-20 days ฿2,502.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(phosphonooxy)propanoic acid
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This chemical is primarily utilized in the field of peptide synthesis, where it serves as a crucial building block for the incorporation of phosphoserine residues into peptides. Its Fmoc-protected amino acid structure allows for selective deprotection during solid-phase peptide synthesis, enabling the precise construction of phosphopeptides. These phosphopeptides are essential tools in biochemical research, particularly in studying protein phosphorylation, signal transduction pathways, and enzyme-substra

This chemical is primarily utilized in the field of peptide synthesis, where it serves as a crucial building block for the incorporation of phosphoserine residues into peptides. Its Fmoc-protected amino acid structure allows for selective deprotection during solid-phase peptide synthesis, enabling the precise construction of phosphopeptides. These phosphopeptides are essential tools in biochemical research, particularly in studying protein phosphorylation, signal transduction pathways, and enzyme-substrate interactions. Additionally, the compound is employed in the development of peptide-based drugs and diagnostics, where phosphorylation plays a critical role in modulating biological activity. Its application extends to the preparation of affinity ligands for purifying phosphorylated proteins and antibodies, aiding in proteomics and immunology studies.

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