3-Amino-4-fluorobenzamide

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Reagent Code: #129238
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CAS Number 943743-25-7

science Other reagents with same CAS 943743-25-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.14 g/mol
Formula C₇H₇FN₂O
badge Registry Numbers
MDL Number MFCD09728800
thermostat Physical Properties
Boiling Point 277.8±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.344±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, which allow for easy modification and incorporation into larger bioactive molecules. Its fluorinated aromatic structure enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in research settings for designing compounds targeting neurological disorders and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,770.00
inventory 5g
10-20 days ฿32,990.00

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3-Amino-4-fluorobenzamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, which allow for easy modification and incorporation into larger bioactive molecules. Its fluorinated aromatic structure enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in research settings for designing compound

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, which allow for easy modification and incorporation into larger bioactive molecules. Its fluorinated aromatic structure enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in research settings for designing compounds targeting neurological disorders and inflammatory diseases.

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