Methyl 2,5-difluoronicotinate

≥95%

Reagent Code: #115390
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CAS Number 1214362-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.12 g/mol
Formula C₇H₅F₂NO₂
badge Registry Numbers
MDL Number MFCD14698038
thermostat Physical Properties
Boiling Point 218.9±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Methyl 2,5-difluoronicotinate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine atoms and a nicotinate moiety, makes it valuable for constructing complex molecules with enhanced biological activity. In medicinal chemistry, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs), especially those targeting central nervous system disorders or infectious diseases. Additionally, its fluorinated aromatic ring contributes to improved metabolic stability and bioavailability in drug candidates. In agrochemical research, it is utilized to develop novel pesticides or herbicides with higher efficacy and selectivity. The compound’s versatility in chemical reactions, such as cross-coupling or nucleophilic substitution, further expands its utility in industrial and academic research settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,718.00
inventory 250mg
10-20 days ฿4,617.00
Methyl 2,5-difluoronicotinate
Methyl 2,5-difluoronicotinate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine atoms and a nicotinate moiety, makes it valuable for constructing complex molecules with enhanced biological activity. In medicinal chemistry, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs), especially those targeting central nervous system disorders or infectious diseases. Additionally, its fluorinated aromatic ring contributes to improved metabolic stability and bioavailability in drug candidates. In agrochemical research, it is utilized to develop novel pesticides or herbicides with higher efficacy and selectivity. The compound’s versatility in chemical reactions, such as cross-coupling or nucleophilic substitution, further expands its utility in industrial and academic research settings.
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