Exploring the Chemical Properties of 2,5-Difluoro-4-(trifluoromethyl)aniline: A Synthesis Intermediate
NINGBO INNO PHARMCHEM CO.,LTD. provides essential chemical intermediates that form the backbone of modern scientific and industrial advancements. Among these, 2,5-difluoro-4-(trifluoromethyl)aniline, identified by CAS Number 114973-22-7, is a compound of significant interest due to its unique chemical profile. This article aims to shed light on the fundamental trifluoromethylaniline chemical properties that make it such a valuable synthesis intermediate.
The molecular formula for 2,5-difluoro-4-(trifluoromethyl)aniline is C7H4F5N. Its molecular weight is approximately 197.105 g/mol. These parameters are critical for stoichiometric calculations in synthesis reactions. The compound's boiling point is reported as 185.3 ± 40.0 °C at 760 mmHg, indicating its stability under standard processing conditions. Furthermore, its density is 1.5 ± 0.1 g/cm³, providing important physical data for handling and formulation.
The presence of two fluorine atoms and a trifluoromethyl group (-CF3) on the aniline ring significantly influences the compound's reactivity and electronic characteristics. These electron-withdrawing groups affect the electron density distribution of the aromatic ring, making specific positions more susceptible to electrophilic or nucleophilic attack. This controlled reactivity is what makes it an excellent fluorinated building block for synthesis.
These precise chemical properties are the reason why 2,5-difluoro-4-(trifluoromethyl)aniline is a sought-after intermediate, particularly for applications requiring specific optical and electronic behaviors, such as in the production of 2,5-difluoro-4-(trifluoromethyl)aniline for OLEDs and other photoelectric devices. Researchers looking to buy 2,5-difluoro-4-(trifluoromethyl)aniline online can rely on NINGBO INNO PHARMCHEM CO.,LTD. to provide material with verified specifications, ensuring successful outcomes in their synthetic endeavors.
Perspectives & Insights
Chem Catalyst Pro
“The presence of two fluorine atoms and a trifluoromethyl group (-CF3) on the aniline ring significantly influences the compound's reactivity and electronic characteristics.”
Agile Thinker 7
“These electron-withdrawing groups affect the electron density distribution of the aromatic ring, making specific positions more susceptible to electrophilic or nucleophilic attack.”
Logic Spark 24
“This controlled reactivity is what makes it an excellent fluorinated building block for synthesis.”