The Chemistry Behind 2'-(Trifluoromethyl)acetophenone: Synthesis and Properties
Understanding the fundamental chemistry of key intermediates is crucial for advancing scientific research and industrial processes. 2'-(Trifluoromethyl)acetophenone, identified by its CAS number 17408-14-9, is a significant compound whose unique structural features dictate its broad applicability. As a leading supplier, NINGBO INNO PHARMCHEM CO.,LTD. is dedicated to elucidating the chemical intricacies of such compounds, ensuring our clients have a comprehensive understanding for their synthetic endeavors.
The synthesis of 2'-(Trifluoromethyl)acetophenone often involves reactions that build the acetophenone structure onto a trifluoromethyl-substituted benzene ring. Common routes may include Friedel-Crafts acylation reactions, where an acetyl group is introduced onto the aromatic ring. The presence of the trifluoromethyl group, being a strongly electron-withdrawing substituent, influences the regioselectivity and reactivity of such reactions. This characteristic makes it a valuable trifluoromethyl acetophenone chemical intermediate, enabling specific transformations that might be challenging with unsubstituted analogs.
Key chemical properties of 2'-(Trifluoromethyl)acetophenone include its physical state – typically a clear, colorless to pale yellow liquid – and its molecular formula, C9H7F3O, with a molecular weight of approximately 188.15 g/mol. The trifluoromethyl group (-CF3) is known for its high electronegativity and steric bulk, which significantly affects the compound’s electronic properties and its interaction with other molecules. This makes it an excellent building block for creating molecules with enhanced lipophilicity, metabolic stability, and specific electronic profiles.
When researchers decide to buy 2'-(trifluoromethyl)acetophenone, they are acquiring a versatile reagent. The carbonyl group is susceptible to nucleophilic attack, while the aromatic ring can undergo further substitution reactions, albeit influenced by the electron-withdrawing nature of the CF3 group. This dual reactivity makes 1-[2-(trifluoromethyl)phenyl]ethanone a potent tool for constructing complex organic structures. Its utility in various organic synthesis reactions highlights why it is frequently sought after.
For industries looking for 2-acetylbenzotrifluoride for sale, understanding its properties is key to successful integration into their manufacturing processes. The boiling point, density, and flash point are critical parameters for process design and safety management. Similarly, when considering o-trifluoromethylacetophenone for novel applications, knowledge of its spectroscopic data, such as NMR and IR spectra, can be invaluable for characterization and quality control.
At NINGBO INNO PHARMCHEM CO.,LTD., we ensure that our 2'-(Trifluoromethyl)acetophenone meets high standards of purity and characterization, supporting your research and development needs. Our commitment to providing accurate chemical information empowers chemists to utilize this intermediate effectively in their synthetic strategies.
In summary, the synthesis and intrinsic chemical properties of 2'-(Trifluoromethyl)acetophenone make it a pivotal compound in modern chemistry. NINGBO INNO PHARMCHEM CO.,LTD. is dedicated to supplying this essential intermediate with the quality and data necessary for its successful application.
Perspectives & Insights
Alpha Spark Labs
“The trifluoromethyl group (-CF3) is known for its high electronegativity and steric bulk, which significantly affects the compound’s electronic properties and its interaction with other molecules.”
Future Pioneer 88
“This makes it an excellent building block for creating molecules with enhanced lipophilicity, metabolic stability, and specific electronic profiles.”
Core Explorer Pro
“When researchers decide to buy 2'-(trifluoromethyl)acetophenone, they are acquiring a versatile reagent.”