Pentafluoropropionaldehyde hydrate

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Reagent Code: #225633
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CAS Number 422-63-9

science Other reagents with same CAS 422-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.05(anhy) g/mol
Formula C₃H₃F₅O₂∙xH₂O
badge Registry Numbers
MDL Number MFCD00792902
thermostat Physical Properties
Melting Point 50-54°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and bioavailability in drug molecules. Commonly employed in the production of fluorinated analogs of bioactive compounds, especially in the development of selective enzyme inhibitors. Also utilized in specialty polymer chemistry to introduce fluorinated segments, improving thermal and chemical resistance of materials. Its reactivity allows for efficient derivatization in multi-step organic syntheses, particularly in routes requiring gem-diol functionality with strong electron-withdrawing groups.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,710.00
inventory 5g
10-20 days ฿19,750.00

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Pentafluoropropionaldehyde hydrate
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Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and bioavailability in drug molecules. Commonly employed in the production of fluorinated analogs of bioactive compounds, especially in the development of selective enzyme inhibitors. Also utilized in specialty polymer chemistry to introduce fluorinated segments, improving thermal and chemical resistance of materials. Its reactivity allows for effi

Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and bioavailability in drug molecules. Commonly employed in the production of fluorinated analogs of bioactive compounds, especially in the development of selective enzyme inhibitors. Also utilized in specialty polymer chemistry to introduce fluorinated segments, improving thermal and chemical resistance of materials. Its reactivity allows for efficient derivatization in multi-step organic syntheses, particularly in routes requiring gem-diol functionality with strong electron-withdrawing groups.

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