2-Amino-5-fluoro-3-methoxy-benzoic acid

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Reagent Code: #42682
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CAS Number 1250810-28-6

science Other reagents with same CAS 1250810-28-6

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Weight 185.1524 g/mol
Formula C₈H₈FNO₃
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MDL Number MFCD14683484
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This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting various therapeutic areas, including anti-inflammatory and anticancer agents. Its structure allows for modifications that enhance the biological activity and selectivity of the final drug molecules. Additionally, it is utilized in research settings for the development of novel chemical entities, aiding in the discovery of new treatments for complex diseases. Its fluorinated and methoxy groups contribute to its utility in creating compounds with improved pharmacokinetic properties.

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inventory 100mg
10-20 days ฿5,292.00

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2-Amino-5-fluoro-3-methoxy-benzoic acid
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This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting various therapeutic areas, including anti-inflammatory and anticancer agents. Its structure allows for modifications that enhance the biological activity and selectivity of the final drug molecules. Additionally, it is utilized in research settings for the development of novel chemica

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting various therapeutic areas, including anti-inflammatory and anticancer agents. Its structure allows for modifications that enhance the biological activity and selectivity of the final drug molecules. Additionally, it is utilized in research settings for the development of novel chemical entities, aiding in the discovery of new treatments for complex diseases. Its fluorinated and methoxy groups contribute to its utility in creating compounds with improved pharmacokinetic properties.

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