4-(Difluoromethyl)-3-fluoropyridin-2-amine

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Reagent Code: #176016
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CAS Number 1804438-73-0

science Other reagents with same CAS 1804438-73-0

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scatter_plot Molecular Information
Weight 162.11 g/mol
Formula C₆H₅F₃N₂
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MDL Number MFCD25476918
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and fungicides. Its fluorinated pyridine structure enhances bioavailability and target specificity in crop protection agents. Also explored in pharmaceutical research for its potential in creating fluorine-containing bioactive molecules, where the difluoromethyl group improves metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,910.00
inventory 250mg
10-20 days ฿15,870.00
inventory 1g
10-20 days ฿57,540.00

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4-(Difluoromethyl)-3-fluoropyridin-2-amine
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and fungicides. Its fluorinated pyridine structure enhances bioavailability and target specificity in crop protection agents. Also explored in pharmaceutical research for its potential in creating fluorine-containing bioactive molecules, where the difluoromethyl group improves metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and fungicides. Its fluorinated pyridine structure enhances bioavailability and target specificity in crop protection agents. Also explored in pharmaceutical research for its potential in creating fluorine-containing bioactive molecules, where the difluoromethyl group improves metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

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