Methyl 2,5-difluoronicotinate
≥95%
Reagent
Code: #115390
CAS Number
1214362-39-6
blur_circular Chemical Specifications
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Molecular Information
Weight
173.12 g/mol
Formula
C₇H₅F₂NO₂
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Registry Numbers
MDL Number
MFCD14698038
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Physical Properties
Boiling Point
218.9±40.0°C at 760 mmHg
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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.
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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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