2-(Trifluoromethoxy)benzaldehyde

96%

Reagent Code: #240031
label
Alias 2-(trifluoromethoxy)benzaldehyde;
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CAS Number 94651-33-9

science Other reagents with same CAS 94651-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₈H₅F₃O₂
badge Registry Numbers
MDL Number MFCD00042405
thermostat Physical Properties
Boiling Point 77 °C20 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.332 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds which exhibit enhanced metabolic stability and bioavailability. Its electron-withdrawing trifluoromethoxy group makes it valuable in the construction of heterocyclic systems and in medicinal chemistry for modifying aromatic scaffolds. Commonly employed in the preparation of antifungal agents, anti-inflammatory drugs, and selective enzyme inhibitors. Also utilized in the fragrance industry due to its aromatic aldehyde functionality, contributing to the design of novel scent molecules with improved stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿660.00
inventory 25g
10-20 days ฿2,630.00
inventory 100g
10-20 days ฿10,260.00

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2-(Trifluoromethoxy)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds which exhibit enhanced metabolic stability and bioavailability. Its electron-withdrawing trifluoromethoxy group makes it valuable in the construction of heterocyclic systems and in medicinal chemistry for modifying aromatic scaffolds. Commonly employed in the preparation of antifungal agents, anti-inflammatory drugs, and selective enzyme inhibitors. Also utilized in t

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds which exhibit enhanced metabolic stability and bioavailability. Its electron-withdrawing trifluoromethoxy group makes it valuable in the construction of heterocyclic systems and in medicinal chemistry for modifying aromatic scaffolds. Commonly employed in the preparation of antifungal agents, anti-inflammatory drugs, and selective enzyme inhibitors. Also utilized in the fragrance industry due to its aromatic aldehyde functionality, contributing to the design of novel scent molecules with improved stability.

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