N-(4-(Trifluoromethyl)phenyl)pivalamide

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Reagent Code: #218119
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CAS Number 25617-34-9

science Other reagents with same CAS 25617-34-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.24 g/mol
Formula C₁₂H₁₄F₃NO
badge Registry Numbers
MDL Number MFCD03094126
thermostat Physical Properties
Boiling Point 327.7±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports metabolic stability due to the trifluoromethyl group, enhancing bioavailability in drug candidates. Also employed in agrochemical research for designing herbicides and fungicides, where the pivalamide moiety contributes to improved lipophilicity and membrane penetration. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,080.00
inventory 25g
10-20 days ฿2,660.00
inventory 50g
10-20 days ฿5,280.00
inventory 100g
10-20 days ฿7,680.00

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N-(4-(Trifluoromethyl)phenyl)pivalamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports metabolic stability due to the trifluoromethyl group, enhancing bioavailability in drug candidates. Also employed in agrochemical research for designing herbicides and fungicides, where the pivalamide moiety contributes to improved lipophilicity and membrane penetration. Commonly utilized in medicinal chemistry for structure-activity relat

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports metabolic stability due to the trifluoromethyl group, enhancing bioavailability in drug candidates. Also employed in agrochemical research for designing herbicides and fungicides, where the pivalamide moiety contributes to improved lipophilicity and membrane penetration. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds.

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