2-(1,1,2,2-Tetrafluoroethoxy)aniline, with the CAS number 35295-34-2, is an organic compound characterized by the presence of both an aniline group and a tetrafluoroethoxy substituent. The molecular structure features a benzene ring attached to an amino group (–NH2) and an ether group containing a tetrafluoroethane moiety, which contributes to its unique chemical properties. This compound is likely to exhibit low volatility and high thermal stability due to the presence of fluorine atoms, which can enhance its resistance to degradation. Additionally, the fluorinated ether group may impart hydrophobic characteristics, affecting its solubility in various solvents. The aniline portion of the molecule can participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic reactions, making it a versatile intermediate in organic synthesis. Its potential applications may span across pharmaceuticals, agrochemicals, and materials science, particularly in the development of fluorinated compounds with specific functional properties. Safety and handling precautions should be observed due to the potential toxicity associated with aniline derivatives.

2-(1,1,2,2-tetrafluoroethoxy)aniline

35295-34-2: 2-(1,1,2,2-Tetrafluoroethoxy)aniline, with the CAS number 35295-34-2, is an organic compound characterized by the presence of both an aniline group and a tetrafluoroethoxy substituent. The molecular structure features a benzene ring attached to an amino group (–NH2) and an ether group containing a tetrafluoroethane moiety, which contributes to its unique chemical properties. This compound is likely to exhibit low volatility and high thermal stability due to the presence of fluorine atoms, which can enhance its resistance to degradation. Additionally, the fluorinated ether group may impart hydrophobic characteristics, affecting its solubility in various solvents. The aniline portion of the molecule can participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic reactions, making it a versatile intermediate in organic synthesis. Its potential applications may span across pharmaceuticals, agrochemicals, and materials science, particularly in the development of fluorinated compounds with specific functional properties. Safety and handling precautions should be observed due to the potential toxicity associated with aniline derivatives.

CAS 35295-34-2

2-(1,1,2,2-tetrafluoroethoxy)aniline

2-(1,1,2,2-Tetrafluoroethoxy)aniline

Ref: 10-F010529

2-(2H-Tetrafluoroethoxy)aniline

Ref: 54-PC5839