methyl 2-fluoro-6-methoxynicotinate

≥95%

Reagent Code: #209969
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CAS Number 117671-03-1

science Other reagents with same CAS 117671-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.15 g/mol
Formula C₈H₈FNO₃
thermostat Physical Properties
Melting Point 81-82℃
Boiling Point 247.1±40.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.244±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing fluorinated heterocyclic compounds. The presence of fluorine enhances metabolic stability and binding affinity in drug candidates. It is also employed in agrochemical research for designing new pesticides and herbicides with improved efficacy and environmental profiles. Commonly utilized in cross-coupling reactions and nucleophilic substitutions to build complex molecules in both academic and industrial settings.

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inventory 1g
10-20 days ฿38,180.00

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methyl 2-fluoro-6-methoxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing fluorinated heterocyclic compounds. The presence of fluorine enhances metabolic stability and binding affinity in drug candidates. It is also employed in agrochemical research for designing new pesticides and herbicides with improved efficacy and e

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing fluorinated heterocyclic compounds. The presence of fluorine enhances metabolic stability and binding affinity in drug candidates. It is also employed in agrochemical research for designing new pesticides and herbicides with improved efficacy and environmental profiles. Commonly utilized in cross-coupling reactions and nucleophilic substitutions to build complex molecules in both academic and industrial settings.

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