3,4-Difluoronitrobenzene possesses a unique chemical structure characterized by a benzene ring substituted with two fluorine atoms at the 3 and 4 positions, along with a nitro group (-NO2) attached to the ring. This compound possesses notable reactivity due to the electron-withdrawing nature of both the fluorine and nitro groups. The presence of these substituents causes an increase in electrophilicity, making the benzene ring more susceptible to nucleophilic attack. Therefore, 3,4-difluoronitrobenzene serves as a valuable intermediate in the synthesis of various complex compounds, particularly those with pharmacological applications.
- Its physical properties include a melting point of approximately 48 degrees Celsius and a boiling point of roughly 188 degrees Celsius.
- Furthermore, it possesses limited solubility in water but is miscible in common organic solvents.
The synthesis of 3,4-difluoronitrobenzene typically comprises a multi-step process wherein includes the nitration of fluorobenzene followed by precise fluorination. This compound has been widely studied due to its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Synthesis and Properties of 3,4-Difluoronitrobenzene
3,4-Difluoronitrobenzene possesses a significant role in the realm of organic synthesis due to its unique structural characteristics. The synthesis of this compound can be achieved through various get more info routes, with a commonly employed method involving the nitration of 1,2-difluorobenzene. This reaction typically utilizes a mixture of nitric acid and sulfuric acid as the nitrating agent, yielding the desired 3,4-difluoronitrobenzene product.
The resulting compound exhibits distinct physicochemical properties that influence its reactivity and applications. Notably, the electron-withdrawing nature of the nitro group in 3,4-difluoronitrobenzene alters its electrophilicity, making it susceptible to nucleophilic attack. This property renders it a versatile building block for the synthesis of complex organic molecules.
- Furthermore, the presence of fluorine atoms in the molecule contributes to its resilience and solubility in various solvents.
CAS No. for 3,4-Difluoronitrobenzene: Identifying This Compound
When working with chemicals, accurately pinpointing them is crucial for safety and correct results. A key tool in this process is the CAS Registry Number, a unique identifier assigned to every chemical compound. For 3,4-Difluoronitrobenzene, this number is vital for ensuring you are working with the correct substance.
The CAS No. for 3,4-Difluoronitrobenzene is 105387-96-3. This unique identifier can be used to locate information about the compound in databases and research materials. Understanding its properties, hazards, and safe handling procedures is crucial when dealing with this chemical.
Applications of 3,4-Difluoronitrobenzene in Research
3,4-Difluoronitrobenzene finds a extensive variety of applications in research. Its unique structure and electronic properties permit it to be utilized as a valuable intermediate in the synthesis of sophisticated organic compounds. Researchers utilize 3,4-difluoronitrobenzene for its adaptability in producing new materials with desired properties. Furthermore, this substance functions as a valuable resource in the study of physical processes. Its capabilities extend various research areas, including materials science.
Safety Considerations for Handling 3,4-Difluoronitrobenzene
When manipulating 3,4-difluoronitrobenzene, it is vital to prioritize risk mitigation. This compound can be dangerous if not handled properly. Always perform operations in a well-ventilated area and wear appropriate safety gear, including gloves, safety glasses, and a protective smock.
Before interacting with with 3,4-difluoronitrobenzene, meticulously review the hazard information provided by the manufacturer. This resource will provide specific guidance on potential threats, first response, and containment procedures.
- Steer clear of contact with eyes. In the event of incidence, immediately flush the region with plenty of water for at least quarter hour.
- Keep 3,4-difluoronitrobenzene in a tempered place away from flammables and hazardous compounds.
- Remove of 3,4-difluoronitrobenzene properly in accordance with applicable laws.
Spectral Characterization of 3,4-Difluoronitrobenzene
The spectral characterization of this fluorinated nitroarene is crucial for comprehending its chemical properties and potential applications.
IR|UV-Vis|NMR spectroscopy provides valuable data into the vibrational modes, electronic transitions, and nuclear structure of this compound.
The characteristic spectral features observed can be attributed to the presence of the nitro group, fluorine atoms, and benzene ring. Intensive spectral analysis reveals the influence of these substituents on the overall molecular environment.
This in-depth spectral characterization contributes our knowledge of DFNB and its potential function in various chemical reactions.