2-Chloro-N-(2-(trifluoromethyl)phenyl)acetamide

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Reagent Code: #161929
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CAS Number 3792-04-9

science Other reagents with same CAS 3792-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.61 g/mol
Formula C₉H₇ClF₃NO
badge Registry Numbers
MDL Number MFCD00018893
thermostat Physical Properties
Boiling Point 331.1±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for more complex molecules due to the reactivity of the chloroacetamide group and the electron-withdrawing trifluoromethylphenyl moiety. Commonly employed in medicinal chemistry for structure-activity relationship studies. Also utilized in agrochemical research for designing bioactive compounds with enhanced stability and lipophilicity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,160.00
inventory 10g
10-20 days ฿20,260.00
inventory 25g
10-20 days ฿40,510.00
inventory 5g
10-20 days ฿13,720.00

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2-Chloro-N-(2-(trifluoromethyl)phenyl)acetamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for more complex molecules due to the reactivity of the chloroacetamide group and the electron-withdrawing trifluoromethylphenyl moiety. Commonly employed in medicinal chemistry for structure-activity relationship studies. Also utilized in agrochemical research for designing bioactive compounds with enhanced stability and lipophilicity.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block for more complex molecules due to the reactivity of the chloroacetamide group and the electron-withdrawing trifluoromethylphenyl moiety. Commonly employed in medicinal chemistry for structure-activity relationship studies. Also utilized in agrochemical research for designing bioactive compounds with enhanced stability and lipophilicity.

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