4-(Difluoromethoxy)-2-fluorobenzaldehyde

98%

Reagent Code: #178070
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CAS Number 1214358-05-0

science Other reagents with same CAS 1214358-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₈H₅F₃O₂
badge Registry Numbers
MDL Number MFCD11847162
thermostat Physical Properties
Boiling Point 222.2±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde functionality allows for facile derivatization, enabling incorporation into larger molecular frameworks. Commonly employed in cross-coupling reactions and condensation processes to build complex aromatic systems found in bioactive molecules. Valued in medicinal chemistry for enabling structure-activity relationship (SAR) studies due to the strategic placement of fluorine atoms and the reactive aldehyde group.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,980.00
inventory 5g
10-20 days ฿10,350.00
inventory 25g
10-20 days ฿43,110.00

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4-(Difluoromethoxy)-2-fluorobenzaldehyde
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde functionality allows for facile derivatization, enabling incorporation into larger molecular frameworks. Commonly employed in cross-coupling reactions and condensation processes to build complex aromatic systems found in bioactive molecules. Valued

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde functionality allows for facile derivatization, enabling incorporation into larger molecular frameworks. Commonly employed in cross-coupling reactions and condensation processes to build complex aromatic systems found in bioactive molecules. Valued in medicinal chemistry for enabling structure-activity relationship (SAR) studies due to the strategic placement of fluorine atoms and the reactive aldehyde group.

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