2,3,4,5,6-Pentafluoroanilino(oxo)acetic acid

95%

Reagent Code: #226660
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CAS Number 1454681-04-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.10 g/mol
Formula C₈H₂F₅NO₃
badge Registry Numbers
MDL Number MFCD26160025
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its highly fluorinated aromatic structure enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in drug design, especially for central nervous system agents and enzyme inhibitors. It also serves in the development of specialty materials, including fluorinated ligands for catalysis and functional polymers with improved thermal and oxidative resistance. The compound’s reactivity allows for peptide coupling and heterocycle formation, enabling its use in combinatorial chemistry and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,130.00

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2,3,4,5,6-Pentafluoroanilino(oxo)acetic acid
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Used primarily as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its highly fluorinated aromatic structure enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in drug design, especially for central nervous system agents and enzyme inhibitors. It also serves in the development of specialty materials, including fluorinated ligands for catalysis and functional polymers with improved thermal and oxidative resistance. The compound’s rea

Used primarily as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its highly fluorinated aromatic structure enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in drug design, especially for central nervous system agents and enzyme inhibitors. It also serves in the development of specialty materials, including fluorinated ligands for catalysis and functional polymers with improved thermal and oxidative resistance. The compound’s reactivity allows for peptide coupling and heterocycle formation, enabling its use in combinatorial chemistry and medicinal chemistry research.

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