3-(Trifluoromethyl)benzaldehyde

97%

Reagent Code: #239887
label
Alias 3-(trifluoromethyl)benzaldehyde; m-trifluoromethylbenzaldehyde
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CAS Number 454-89-7

science Other reagents with same CAS 454-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.12 g/mol
Formula C₈H₅F₃O
badge Registry Numbers
EC Number 207-228-1
MDL Number MFCD00003373
thermostat Physical Properties
Boiling Point 83-86 °C30 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.301 g/mL at 25 °C(lit.)
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants and antipsychotic drugs. It serves as a building block in agrochemicals for developing herbicides and fungicides due to the stability and lipophilicity imparted by the trifluoromethyl group. Also employed in the manufacture of dyes and fluorescent compounds, where it contributes to enhanced photostability and electronic properties. Its aldehyde functionality allows for easy modification in organic reactions, making it valuable in research and development of new bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿370.00
inventory 25g
10-20 days ฿450.00
inventory 100g
10-20 days ฿1,750.00
inventory 500g
10-20 days ฿8,600.00

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3-(Trifluoromethyl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants and antipsychotic drugs. It serves as a building block in agrochemicals for developing herbicides and fungicides due to the stability and lipophilicity imparted by the trifluoromethyl group. Also employed in the manufacture of dyes and fluorescent compounds, where it contributes to enhanced photostability and electronic properties. Its aldehyde functionality allows for easy modification in or

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antidepressants and antipsychotic drugs. It serves as a building block in agrochemicals for developing herbicides and fungicides due to the stability and lipophilicity imparted by the trifluoromethyl group. Also employed in the manufacture of dyes and fluorescent compounds, where it contributes to enhanced photostability and electronic properties. Its aldehyde functionality allows for easy modification in organic reactions, making it valuable in research and development of new bioactive molecules.

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