2-Methyl-3-(trifluoromethyl)benzaldehyde

97%

Reagent Code: #205302
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CAS Number 878001-20-8

science Other reagents with same CAS 878001-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.15 g/mol
Formula C₉H₇F₃O
badge Registry Numbers
MDL Number MFCD04116032
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for anti-inflammatory and central nervous system drugs. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Also employed in agrochemicals for developing herbicides and fungicides due to the stability and reactivity imparted by the trifluoromethyl group. Additionally, it serves as a building block in the preparation of specialty chemicals, including dyes and fluorescent compounds, where the aldehyde group enables coupling reactions for extended conjugation systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿890.00
5g
10-20 days ฿4,160.00
2-Methyl-3-(trifluoromethyl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for anti-inflammatory and central nervous system drugs. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Also employed in agrochemicals for developing herbicides and fungicides due to the stability and reactivity imparted by the trifluoromethyl group. Additionally, it serves as a building block in the preparation of specialty c

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for anti-inflammatory and central nervous system drugs. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Also employed in agrochemicals for developing herbicides and fungicides due to the stability and reactivity imparted by the trifluoromethyl group. Additionally, it serves as a building block in the preparation of specialty chemicals, including dyes and fluorescent compounds, where the aldehyde group enables coupling reactions for extended conjugation systems.

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