Apollo Scientific

Fluorochem

Indagoo

2,6-Difluoro-3-hydroxybenzamide is an organic compound characterized by the presence of a benzene ring substituted with two fluorine atoms and a hydroxyl group, along with an amide functional group. The fluorine atoms are located at the 2 and 6 positions of the benzene ring, while the hydroxyl group is positioned at the 3 position, contributing to the compound's unique reactivity and properties. This compound is likely to exhibit polar characteristics due to the presence of the hydroxyl group, which can engage in hydrogen bonding, influencing its solubility in polar solvents. The fluorine substituents can enhance the compound's lipophilicity and stability, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the presence of both electron-withdrawing (fluorine) and electron-donating (hydroxyl) groups can affect the compound's electronic properties, potentially influencing its biological activity. Overall, 2,6-Difluoro-3-hydroxybenzamide represents a versatile structure with potential applications in medicinal chemistry and materials science.

2,6-Difluoro-3-hydroxybenzaMide

951122-37-5: 2,6-Difluoro-3-hydroxybenzamide is an organic compound characterized by the presence of a benzene ring substituted with two fluorine atoms and a hydroxyl group, along with an amide functional group. The fluorine atoms are located at the 2 and 6 positions of the benzene ring, while the hydroxyl group is positioned at the 3 position, contributing to the compound's unique reactivity and properties. This compound is likely to exhibit polar characteristics due to the presence of the hydroxyl group, which can engage in hydrogen bonding, influencing its solubility in polar solvents. The fluorine substituents can enhance the compound's lipophilicity and stability, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the presence of both electron-withdrawing (fluorine) and electron-donating (hydroxyl) groups can affect the compound's electronic properties, potentially influencing its biological activity. Overall, 2,6-Difluoro-3-hydroxybenzamide represents a versatile structure with potential applications in medicinal chemistry and materials science.

CAS 951122-37-5

2,6-Difluoro-3-hydroxybenzaMide

2,6-Difluoro-3-hydroxybenzamide

Ref: 10-F620094

2,6-Difluoro-3-hydroxybenzamide

Ref: 54-PC48578

Benzamide, 2,6-difluoro-3-hydroxy-

Ref: IN-DA006PT0

2,6-Difluoro-3-hydroxybenzamide

Ref: IN-DG286829