3,4-Difluoro nitrobenzene is a fluorinated benzene derivative with the chemical structure C₆H₃F₂NO₂. It's a cream colored solid at standard conditions. This compound exhibits interesting properties making it valuable in various applications.

During its synthesis, 3,4-difluoro nitrobenzene involves a series of reactions. The most common method utilizes fluorination agents to introduce fluorine atoms into the benzene ring. This is followed by a nitration reaction to yield the desired product.

Notable features associated with 3,4-difluoro nitrobenzene include its high melting point. It also demonstrates a tendency to participate in specific reactions. These properties make it efficient in various applications such as pharmaceutical intermediates.

3,4-Difluoro nitrobenzene: A Versatile Building Block in Organic Synthesis

3,4-Difluoro nitrobenzene, the highly valuable intermediate, plays an important part in the realm of organic synthesis. Its unique structure allows for multiple chemical transformations, making it a flexible building block for synthesizing complex organic molecules.

• Many synthetic methodologies have been explored to utilize 3,4-difluoro nitrobenzene in the preparation of diverse target compounds.
• , As an illustration , it can be used as a precursor for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

The fluoroine atoms present in 3,4-difluoro nitrobenzene can be easily modified, further enhancing its utility as a synthetic tool.

Analytical Characterization of 3,4-Difluoro Nitrobenzene

Analytical characterization of substance 3,4-difluoro nitrobenzene is a crucial step in understanding its physicochemical properties and potential applications. Various analytical techniques can be employed to analyze the structure, purity, and properties of this substance. Commonly used methods include {nuclear magnetic resonance (NMR) spectroscopy|infrared (IR) spectroscopy , which provide information about its structure and functional groups. Additionally , techniques such as gas chromatography-mass spectrometry (GC-MS) or high-performance liquid chromatography-mass spectrometry (HPLC-MS) can be used to determine the concentration of 3,4-difluoro nitrobenzene in a mixture.

Through these analytical techniques, we can gain valuable understanding about the properties and behavior of this compound, which is essential for its safe and effective utilization.

Safety Considerations for Handling 3,4-Difluoro Nitrobenzene

When manipulating 3,4-difluoro nitrobenzene, rigorous safety protocols are critical. This material can be dangerous if inhaled. Always employ appropriate personal protective equipment, including gloves, a respirator, and vision protection. Conduct operations in a well-ventilated area and avoid exposure with skin, eyes, and clothing. In case of spills, follow established protocols for removal.

• Store 3,4-difluoro nitrobenzene in a regulated location away from reactive materials.
• Eliminate of waste properly according to applicable regulations.
• Refer to the material safety data sheet (MSDS) for thorough information on handling and storage.

The CAS No. and Chemical Identity of 3,4-Difluoro Nitrobenzene

3,4-Difluoro nitrobenzene is a synthetic organic molecule with the CAS No. 124295-97-2. Its molecular formula consists of a benzene ring decorated with two fluorine atoms at the 3 and 4 positions, as well as a nitro group (-NO₂) attached to the ring. This material is often employed in the production of various agrochemicals.

Applications of 3,4-Difluoro Nitrobenzene in Pharmaceutical Research

3,4-Difluoro nitrobenzene serves a versatile building block within the realm of pharmaceutical development. Due to its unique structural properties, this compound has emerged as a key element in the creation of various therapeutic agents. Scientists are increasingly investigating its potential in the development of drugs targeting a broad range of conditions.

One notable application lies in the field of germicidal agents, where 3,4-difluoro nitrobenzene analogs have demonstrated remarkable activity against a range of pathogenic microbes. Furthermore, its potential in the alleviation of immune-related disorders 3 4 difluoronitrobenzene cas no is actively investigated.

The molecular versatility of 3,4-difluoro nitrobenzene allows for multiple modifications and linkages, enabling the synthesis of novel compounds with tailored characteristics. This versatility makes it a valuable tool in the ongoing quest to develop effective and safe pharmaceuticals.