N,N-Dimethyl-4-(trifluoromethyl)benzamide

98%

Reagent Code: #218818
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CAS Number 25771-21-5

science Other reagents with same CAS 25771-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.19 g/mol
Formula C₁₀H₁₀F₃NO
badge Registry Numbers
MDL Number MFCD16618942
thermostat Physical Properties
Boiling Point 276.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates. Also employed in agrochemical research for designing herbicides and fungicides due to its electron-withdrawing properties and resistance to degradation. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to improve potency and bioavailability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,390.00
inventory 1g
10-20 days ฿3,470.00
inventory 5g
10-20 days ฿10,800.00

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N,N-Dimethyl-4-(trifluoromethyl)benzamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates. Also employed in agrochemical research for designing herbicides and fungicides due to its electron-withdrawing properties and resistance to degradation. Commonly utilized in medicinal chemistry for structure-activity relationship (SA

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates. Also employed in agrochemical research for designing herbicides and fungicides due to its electron-withdrawing properties and resistance to degradation. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to improve potency and bioavailability.

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