2-(Trifluoromethyl)benzaldehyde

98%

Reagent Code: #239630
label
Alias o-trifluoromethylbenzaldehyde;2-trifluoromethylbenzaldehyde
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CAS Number 447-61-0

science Other reagents with same CAS 447-61-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.12 g/mol
Formula C₈H₅F₃O
badge Registry Numbers
EC Number 207-185-9
MDL Number MFCD00003337
thermostat Physical Properties
Melting Point -40 °C
Boiling Point 70-71 °C (16 mmHg)
inventory_2 Storage & Handling
Density 1.32 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and antimicrobial agents. Its electrophilic aldehyde group and electron-withdrawing trifluoromethyl substituent make it valuable in constructing complex organic molecules through reactions like condensation, reduction, and nucleophilic addition. Commonly employed in the development of agrochemicals and functional materials due to the stability and lipophilicity imparted by the trifluoromethyl group. Also utilized in the preparation of liquid crystals and fluorescent dyes where fluorinated aromatic aldehydes enhance optical and electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿260.00
inventory 25g
10-20 days ฿360.00
inventory 100g
10-20 days ฿1,330.00
inventory 500g
10-20 days ฿6,360.00

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2-(Trifluoromethyl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and antimicrobial agents. Its electrophilic aldehyde group and electron-withdrawing trifluoromethyl substituent make it valuable in constructing complex organic molecules through reactions like condensation, reduction, and nucleophilic addition. Commonly employed in the development of agrochemicals and functional materials due to the stability and lipophilicity imparted by the trifluorometh

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and antimicrobial agents. Its electrophilic aldehyde group and electron-withdrawing trifluoromethyl substituent make it valuable in constructing complex organic molecules through reactions like condensation, reduction, and nucleophilic addition. Commonly employed in the development of agrochemicals and functional materials due to the stability and lipophilicity imparted by the trifluoromethyl group. Also utilized in the preparation of liquid crystals and fluorescent dyes where fluorinated aromatic aldehydes enhance optical and electronic properties.

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