3,4-Difluoronitrobenzene is 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 generates an increase in electrophilicity, making the benzene ring more susceptible to nucleophilic attack. Consequently, 3,4-difluoronitrobenzene serves as a valuable intermediate in the synthesis of various chemical compounds, particularly those with medical applications.

• Its physical properties include a melting point of roughly 52 degrees Celsius and a boiling point of approximately 190 degrees Celsius.
• Moreover, it possesses limited solubility in water but is dissolvable in common organic solvents.

The synthesis of 3,4-difluoronitrobenzene typically requires a multi-step process that includes the nitration of fluorobenzene followed by selective fluorination. This compound has been extensively investigated due to its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.

Synthesis and Properties of 3,4-Difluoronitrobenzene

3,4-Difluoronitrobenzene is 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, generating 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 modifies 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 durability and dissolvability in various solvents.

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

When working with chemicals, accurately recognizing 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 source materials. Understanding its properties, hazards, and safe handling procedures is crucial when dealing 3 4 difluoronitrobenzene cas no with this chemical.

Applications of 3,4-Difluoronitrobenzene in Research

3,4-Difluoronitrobenzene exhibits a extensive range of applications in research. Its unique arrangement and chemical properties make it to be utilized as a valuable building block in the synthesis of sophisticated organic compounds. Researchers utilize 3,4-difluoronitrobenzene for its adaptability in developing new materials with specific properties. Furthermore, this substance serves as a important reagent in the study of biological phenomena. Its capabilities cover various research areas, including organic chemistry.

Safety Considerations for Handling 3,4-Difluoronitrobenzene

When manipulating 3,4-difluoronitrobenzene, it is vital to prioritize personal protection. This chemical can be dangerous if not treated properly. Always carry out procedures in a well-ventilated region and utilize appropriate protective clothing, including chemical resistant gloves, goggles, and a lab coat.

Before interacting with with 3,4-difluoronitrobenzene, meticulously review the safety information provided by the supplier. This guide will provide specific information on potential risks, first aid, and storage procedures.

• Refrain from contact with skin. In the event of contact, immediately flush the site with copious amounts of clean water for at least fifteen minutes.
• Keep 3,4-difluoronitrobenzene in a cool area away from ignition points and incompatible materials.
• Eliminate of 3,4-difluoronitrobenzene and its containers in accordance with local regulations.

Spectral Characterization of 3,4-Difluoronitrobenzene

Comprehensive spectral characterization of DFNB is crucial for understanding its chemical properties and potential applications.

Infrared|UV-Vis|NMR spectroscopy provides valuable data into the vibrational modes, electronic transitions, and atomic structure of this compound.

The distinct spectral features observed may be related to the presence of the nitro group, fluorine atoms, and benzene ring. Further spectral analysis highlights the influence of these substituents on the overall molecular structure.

This detailed spectral characterization improves our understanding of DFNB and its potential role in various chemical reactions.