3'-nitro-5'-(trifluoromethyl)acetophenone
$300.00
CAS No.: 39174-87-3
Catalog No.: WLZ1724
Purity: 95%
MF: C9H6F3NO3
MW: 233.145
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C=1C=C(C=C(C1)C(F)(F)F)C(C)=O
Catalog No.: WLZ1724
Purity: 95%
MF: C9H6F3NO3
MW: 233.145
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C=1C=C(C=C(C1)C(F)(F)F)C(C)=O
CAS NO.: 39174-87-3; 3'-nitro-5'-(trifluoromethyl)acetophenone. PROPERTIES: This nitrotrifluoromethyl aromatic ketone features a nitro group and a trifluoromethyl group on a phenyl ring connected to an acetone group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 3'-nitro-5'-(trifluoromethyl)acetophenone typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing nitro and trifluoromethyl groups 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 3'-nitro-5'-(trifluoromethyl)acetophenone serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The ketone group provides a handle for further functionalization through reactions such as reduction or nucleophilic addition. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The trifluoromethyl and nitro substituents contribute to target binding affinity and selectivity. 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 defined substitution pattern, enabling the development of advanced materials with tailored electronic characteristics.
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