3,4-Difluoronitrobenzene exhibits 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 demonstrates 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 chemical compounds, particularly those with biological applications.

• Its physical properties include a melting point of around 50 degrees Celsius and a boiling point of roughly 188 degrees Celsius.
• Furthermore, it possesses limited solubility in water but is soluble in common organic solvents.

The synthesis of 3,4-difluoronitrobenzene typically involves a multi-step process wherein includes the nitration of fluorobenzene followed by precise fluorination. This compound has been thoroughly examined 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 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 website and applications. Notably, the electron-withdrawing nature of the nitro group in 3,4-difluoronitrobenzene modifies its electrophilicity, making it susceptible to nucleophilic attack. This property renders it a versatile building block for the synthesis of complex organic molecules.

• Moreover, the presence of fluorine atoms in the molecule contributes to its resilience and miscibility in various solvents.

CAS No. for 3,4-Difluoronitrobenzene: Identifying This Compound

When working with chemicals, accurately pinpointing them is crucial for safety and precise 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 essential for ensuring you are working with the correct substance.

The CAS No. for 3,4-Difluoronitrobenzene is 105387-96-3. This numerical 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 range of applications in research. Its unique arrangement and chemical properties make it to be utilized as a valuable intermediate in the synthesis of novel organic compounds. Researchers exploit 3,4-difluoronitrobenzene for its reactivity in producing new materials with targeted properties. Furthermore, this compound acts as a important reagent in the study of biological reactions. Its possibilities cover various research areas, including materials science.

Safety Considerations for Handling 3,4-Difluoronitrobenzene

When handling 3,4-difluoronitrobenzene, it is critical to prioritize personal protection. This chemical can be harmful if not managed properly. Always work in a well-ventilated region and utilize appropriate protective clothing, including chemical resistant gloves, eye protection, and a coveralls.

Before coming into contact with 3,4-difluoronitrobenzene, carefully review the safety information provided by the provider. This document will provide specific information on potential hazards, first response, and storage procedures.

• Steer clear of exposure with skin. In the event of incidence, immediately flush the site with a large volume of water for at least fifteen minutes.
• Store 3,4-difluoronitrobenzene in a tempered location away from ignition points and hazardous compounds.
• Eliminate of 3,4-difluoronitrobenzene and its containers in accordance with local regulations.

Spectral Characterization of 3,4-Difluoronitrobenzene

The spectral characterization of DFNB is crucial for elucidating its chemical properties and potential applications.

IR|UV-Vis|NMR spectroscopy provides valuable information into the vibrational modes, electronic transitions, and nuclear structure of this compound.

The pronounced spectral features observed may be assigned to the presence of the nitro group, fluorine atoms, and benzene ring. Intensive spectral analysis demonstrates the influence of these substituents on the overall molecular polarity.

This thorough spectral characterization improves our appreciation of DFNB and its potential application in various chemical reactions.