CAS 350-96-9
:2,2,2-trifluoro-N-(4-methylphenyl)acetamide
Description:
2,2,2-Trifluoro-N-(4-methylphenyl)acetamide, with the CAS number 350-96-9, is an organic compound characterized by its unique trifluoromethyl group and an acetamide functional group. This compound features a trifluoromethyl group (-CF3) attached to the second carbon of the acetamide, which significantly influences its chemical properties, including increased lipophilicity and potential biological activity. The presence of the para-methylphenyl group enhances its steric and electronic characteristics, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The trifluoromethyl group is known for imparting stability and altering the reactivity of the molecule, often leading to enhanced potency in biological systems. In terms of physical properties, it is typically a solid at room temperature, with moderate solubility in organic solvents. Its unique structure allows for potential interactions in biological systems, making it a subject of study in medicinal chemistry. Safety data should be consulted for handling and usage, as fluorinated compounds can exhibit specific toxicological profiles.
Formula:C9H8F3NO
InChI:InChI=1/C9H8F3NO/c1-6-2-4-7(5-3-6)13-8(14)9(10,11)12/h2-5H,1H3,(H,13,14)
SMILES:Cc1ccc(cc1)NC(=O)C(F)(F)F
Synonyms:- acetamide, 2,2,2-trifluoro-N-(4-methylphenyl)-
- 2,2,2-Trifluoro-p-acetotoluidide
- p-Methyltrifluoroacetanilide
- 2,2,2-Trifluoro-N-(4-Methylphenyl)acetaMide
- p-Toluidine Trifluoroacetamide
- NSC 87411
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p-Toluidine Trifluoroacetamide
CAS:Controlled Product<p>Applications p-Toluidine Trifluoroacetamide (cas# 350-96-9) is a compound useful in organic synthesis.<br></p>Formula:C9H8F3NOColor and Shape:NeatMolecular weight:203.16
