2,3,6-Trifluorobenzaldehyde

98%

Reagent Code: #240000
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CAS Number 104451-70-9

science Other reagents with same CAS 104451-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.09 g/mol
Formula F₃C₆H₂CHO
badge Registry Numbers
MDL Number MFCD00061195
thermostat Physical Properties
Boiling Point 159 °C(lit.)
inventory_2 Storage & Handling
Density 1.425 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the polyfluorinated aromatic moiety enhances metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex organic molecules. Commonly employed in the preparation of agrochemicals and functional materials due to the electron-withdrawing effect of fluorine atoms, which influences reactivity and binding properties. Also utilized in the manufacture of liquid crystals and specialty polymers where fluorine substitution improves thermal and chemical resistance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿800.00
inventory 5g
10-20 days ฿3,340.00
inventory 25g
10-20 days ฿16,500.00
2,3,6-Trifluorobenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the polyfluorinated aromatic moiety enhances metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex organic molecules. Commonly employed in the preparation of agrochemicals and functional materials due to the electron-withdrawing effect of fluorine atoms, which influences reactivity and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the polyfluorinated aromatic moiety enhances metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex organic molecules. Commonly employed in the preparation of agrochemicals and functional materials due to the electron-withdrawing effect of fluorine atoms, which influences reactivity and binding properties. Also utilized in the manufacture of liquid crystals and specialty polymers where fluorine substitution improves thermal and chemical resistance.

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