Methyl 2-fluoro-5-methyl-4-nitrobenzoate

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Reagent Code: #42455
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CAS Number 1803736-71-1

science Other reagents with same CAS 1803736-71-1

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Weight 213.1600 g/mol
Formula C₉H₈FNO₄
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MDL Number MFCD28797644
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This chemical is primarily used in organic synthesis as an intermediate in the production of more complex compounds, particularly in pharmaceutical research. It serves as a building block for the development of active pharmaceutical ingredients (APIs) due to its reactive functional groups, which allow for further chemical modifications. The presence of the nitro group makes it useful in reactions involving reduction or substitution, while the ester group provides versatility for hydrolysis or transesterification processes. Additionally, its fluorine atom enhances its potential in the design of bioactive molecules, as fluorine-containing compounds often exhibit improved metabolic stability and binding affinity. This compound is also employed in material science for the synthesis of specialty chemicals and advanced materials.

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inventory 100mg
10-20 days ฿4,545.00

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Methyl 2-fluoro-5-methyl-4-nitrobenzoate
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This chemical is primarily used in organic synthesis as an intermediate in the production of more complex compounds, particularly in pharmaceutical research. It serves as a building block for the development of active pharmaceutical ingredients (APIs) due to its reactive functional groups, which allow for further chemical modifications. The presence of the nitro group makes it useful in reactions involving reduction or substitution, while the ester group provides versatility for hydrolysis or transesteri

This chemical is primarily used in organic synthesis as an intermediate in the production of more complex compounds, particularly in pharmaceutical research. It serves as a building block for the development of active pharmaceutical ingredients (APIs) due to its reactive functional groups, which allow for further chemical modifications. The presence of the nitro group makes it useful in reactions involving reduction or substitution, while the ester group provides versatility for hydrolysis or transesterification processes. Additionally, its fluorine atom enhances its potential in the design of bioactive molecules, as fluorine-containing compounds often exhibit improved metabolic stability and binding affinity. This compound is also employed in material science for the synthesis of specialty chemicals and advanced materials.

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