2-iodo-5-(trifluoromethyl)benzoic acid

2-iodo-5-(trifluoromethyl)benzoic acid

2-fluoro-5-(trifluoromethoxy)aniline

2-fluoro-5-(trifluoromethoxy)aniline

2-fluoro-6-hydroxybenzamide

$200.00
CAS No.: 160748-95-8
Catalog No.: WLZ1660
Purity: 95%
MF: C7H6FNO2
MW: 155.128
Storage: 2-8 degree Celsius
SMILES: FC1=C(C(=O)N)C(=CC=C1)O
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CAS NO.: 160748-95-8; 2-fluoro-6-hydroxybenzamide. PROPERTIES: This fluorinated aromatic amide features a fluorine atom and a hydroxy group on a benzene ring connected to an amide group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2-fluoro-6-hydroxybenzamide typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing amide and fluorine groups and a hydroxy group that influence the electronic properties of the aromatic system. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 2-fluoro-6-hydroxybenzamide serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The amide group provides a handle for further functionalization through reactions such as hydrolysis or amidation. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The hydroxy group can be further modified for additional diversification. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.

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