N-(3,5-Bis(trifluoromethyl)phenyl)-2-chloroacetamide

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Reagent Code: #218929
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CAS Number 790-75-0

science Other reagents with same CAS 790-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.60 g/mol
Formula C₁₀H₆ClF₆NO
badge Registry Numbers
MDL Number MFCD00077474
thermostat Physical Properties
Melting Point 85 °C
Boiling Point 296.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.520±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal and anti-inflammatory properties. Its structure supports use in agrochemicals, where it contributes to the creation of novel pesticides and herbicides due to enhanced stability and reactivity imparted by the trifluoromethyl groups. Also employed in research settings for the design of new fluorinated organic molecules, leveraging its electron-withdrawing characteristics to influence reaction pathways and molecular interactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 5g
10-20 days ฿4,160.00

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N-(3,5-Bis(trifluoromethyl)phenyl)-2-chloroacetamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal and anti-inflammatory properties. Its structure supports use in agrochemicals, where it contributes to the creation of novel pesticides and herbicides due to enhanced stability and reactivity imparted by the trifluoromethyl groups. Also employed in research settings for the design of new fluorinated organic molecules, leveraging its electron-withdrawing characteris

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal and anti-inflammatory properties. Its structure supports use in agrochemicals, where it contributes to the creation of novel pesticides and herbicides due to enhanced stability and reactivity imparted by the trifluoromethyl groups. Also employed in research settings for the design of new fluorinated organic molecules, leveraging its electron-withdrawing characteristics to influence reaction pathways and molecular interactions.

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