(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid

97%

Reagent Code: #38013
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CAS Number 954147-36-5

science Other reagents with same CAS 954147-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.40 g/mol
Formula C₂₀H₁₉N₅O₄
badge Registry Numbers
MDL Number MFCD26407302
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block for the introduction of tetrazole-containing amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide assembly. The tetrazole moiety is of interest due to its bioisosteric properties, often mimicking carboxylic acids or other functional groups in drug design, making it valuable in the development of pharmaceuticals. Its application is crucial in creating peptide-based drugs, enzyme inhibitors, and other bioactive molecules with enhanced stability and specificity.

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

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,041.00
inventory 100mg
10-20 days ฿6,516.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid
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This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block for the introduction of tetrazole-containing amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide assembly. The tetrazole moiety is of interest due to its bioisosteric properties, often mimicking carboxylic acids or other functional groups in drug

This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block for the introduction of tetrazole-containing amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide assembly. The tetrazole moiety is of interest due to its bioisosteric properties, often mimicking carboxylic acids or other functional groups in drug design, making it valuable in the development of pharmaceuticals. Its application is crucial in creating peptide-based drugs, enzyme inhibitors, and other bioactive molecules with enhanced stability and specificity.

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