(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(difluoro(phosphono)methyl)phenyl)propanoic acid

98%

Reagent Code: #236492
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CAS Number 160751-44-0

science Other reagents with same CAS 160751-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 517.42 g/mol
Formula C₂₅H₂₂F₂NO₇P
badge Registry Numbers
MDL Number MFCD01317828
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of phosphorus-containing peptides for biochemical and medicinal research. The difluorophosphonate group mimics natural phosphate esters, making it valuable in designing enzyme inhibitors, especially for proteases and phosphatases involved in cellular signaling. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, allowing mild deprotection conditions. Useful in developing bioactive peptides with enhanced metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,000.00
inventory 100mg
10-20 days ฿18,500.00
inventory 50mg
10-20 days ฿11,900.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(difluoro(phosphono)methyl)phenyl)propanoic acid
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Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of phosphorus-containing peptides for biochemical and medicinal research. The difluorophosphonate group mimics natural phosphate esters, making it valuable in designing enzyme inhibitors, especially for proteases and phosphatases involved in cellular signaling. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, allowing mild deprotection conditions. Useful in developing bioactive peptide

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of phosphorus-containing peptides for biochemical and medicinal research. The difluorophosphonate group mimics natural phosphate esters, making it valuable in designing enzyme inhibitors, especially for proteases and phosphatases involved in cellular signaling. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, allowing mild deprotection conditions. Useful in developing bioactive peptides with enhanced metabolic stability and binding affinity.

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