2,6-Dichloro-4-(trifluoromethyl)benzaldehyde

95%

Reagent Code: #179572
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CAS Number 118754-52-2

science Other reagents with same CAS 118754-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.01 g/mol
Formula C₈H₃Cl₂F₃O
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MDL Number MFCD20441469
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen and trifluoromethyl groups, which enhance biological activity and stability. Also utilized in the preparation of dyes and fluorescent compounds, where the aldehyde group facilitates coupling reactions. Its electron-withdrawing substituents improve reactivity in nucleophilic addition and condensation reactions, useful in fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,070.00
inventory 250mg
10-20 days ฿5,190.00
inventory 1g
10-20 days ฿17,140.00

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2,6-Dichloro-4-(trifluoromethyl)benzaldehyde
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Widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen and trifluoromethyl groups, which enhance biological activity and stability. Also utilized in the preparation of dyes and fluorescent compounds, where the aldehyde group facilitates coupling reactions. Its electron-wit

Widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen and trifluoromethyl groups, which enhance biological activity and stability. Also utilized in the preparation of dyes and fluorescent compounds, where the aldehyde group facilitates coupling reactions. Its electron-withdrawing substituents improve reactivity in nucleophilic addition and condensation reactions, useful in fine chemical manufacturing.

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