4-(Trifluoromethoxy)acetanilide, with the CAS number 1737-06-0, is an organic compound characterized by the presence of both an acetanilide and a trifluoromethoxy group. This compound features a phenyl ring substituted with an acetamide functional group and a trifluoromethoxy group, which significantly influences its chemical properties. The trifluoromethoxy group enhances the compound's lipophilicity and can affect its reactivity and biological activity. Typically, compounds like this exhibit moderate to high stability under standard conditions, but their reactivity can vary based on the presence of functional groups. 4-(Trifluoromethoxy)acetanilide may be used in various applications, including pharmaceuticals and agrochemicals, due to its potential biological activity. Its solubility in organic solvents and limited solubility in water are common characteristics of such compounds, making them suitable for specific chemical reactions and formulations. Safety data should be consulted for handling and usage, as the trifluoromethoxy group can impart unique toxicological properties.

4-(trifluoromethoxy)acetanilide

1737-06-0: p-Acetanisidide, alpha,alpha,alpha-trifluoro-, alpha,alpha,alpha-Trifluoro-p-acetanisidide, N-[4-(trifluoromethoxy)phenyl]acetamide

4'-(Trifluoromethoxy)acetanilide

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CAS 1737-06-0: 4-(trifluoromethoxy)acetanilide

4'-(Trifluoromethoxy)acetanilide

Ref: 54-PC7433C

N-[4-(trifluoromethoxy)phenyl]acetamide

Ref: 3D-FT105580

Riluzole Impurity 6

Ref: 4Z-R-1424

4'-(Trifluoromethoxy)acetanilide

Ref: 10-F007530

Acetamide, N-[4-(trifluoromethoxy)phenyl]-

Ref: IN-DA001Z4M