5-Fluoro-2-oxo-1,2-dihydropyridine-3-carbaldehyde

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Reagent Code: #48550
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CAS Number 917391-98-1

science Other reagents with same CAS 917391-98-1

blur_circular Chemical Specifications

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Weight 141.1000 g/mol
Formula C₆H₄FNO₂
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MDL Number MFCD19227102
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Storage room temperature

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This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure serves as a key intermediate in the creation of molecules that target specific enzymes or pathways involved in disease progression. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, which are valuable in medicinal chemistry for designing novel drugs with improved efficacy and selectivity. Its reactive aldehyde group allows for further functionalization, making it a versatile building block in drug discovery and development processes.

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inventory 100mg
10-20 days ฿6,111.00

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5-Fluoro-2-oxo-1,2-dihydropyridine-3-carbaldehyde
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This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure serves as a key intermediate in the creation of molecules that target specific enzymes or pathways involved in disease progression. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, which are valuable in medicinal chemistry for designing novel drugs with improved efficacy and selectivity. Its react

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure serves as a key intermediate in the creation of molecules that target specific enzymes or pathways involved in disease progression. Additionally, it is employed in organic synthesis to construct complex heterocyclic frameworks, which are valuable in medicinal chemistry for designing novel drugs with improved efficacy and selectivity. Its reactive aldehyde group allows for further functionalization, making it a versatile building block in drug discovery and development processes.

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