6-(Trifluoromethyl)nicotinamide

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Reagent Code: #240705
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CAS Number 386715-35-1

science Other reagents with same CAS 386715-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₇H₅F₃N₂O
thermostat Physical Properties
Melting Point 185-187°C
Boiling Point 270.1°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a building block for bioactive molecules, particularly in the development of drugs targeting neurological and inflammatory conditions. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Also employed in agrochemicals to improve the potency and durability of pesticides. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing properties and ability to influence binding affinity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿470.00
inventory 5g
10-20 days ฿1,670.00
inventory 25g
10-20 days ฿6,010.00

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6-(Trifluoromethyl)nicotinamide
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Used in pharmaceutical research as a building block for bioactive molecules, particularly in the development of drugs targeting neurological and inflammatory conditions. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Also employed in agrochemicals to improve the potency and durability of pesticides. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing

Used in pharmaceutical research as a building block for bioactive molecules, particularly in the development of drugs targeting neurological and inflammatory conditions. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Also employed in agrochemicals to improve the potency and durability of pesticides. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing properties and ability to influence binding affinity.

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