3,4-Difluoro nitrobenzene is a nitroaromatic molecule with the chemical structure C6H3F2NO2. It's a light beige solid at standard conditions. This compound exhibits interesting properties making it essential for diverse fields.
In the production process of 3,4-difluoro nitrobenzene involves a complex procedure. The most common method utilizes fluoride compounds 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 limited chemical activity. These properties make it applicable to applications such as agricultural chemicals.
3,4-Difluoro nitrobenzene: A Versatile Building Block in Organic Synthesis
3,4-Difluoro nitrobenzene, the highly valuable intermediate, plays a crucial role in the realm of organic synthesis. Its remarkable arrangement allows for diverse chemical transformations, making it an adaptable building block for creating complex organic structures.
- Many synthetic methodologies have been refined to utilize 3,4-difluoro nitrobenzene in the preparation of a wide range of target structures.
- , For example , it can be used as a starting material for the synthesis of pharmaceuticals, agrochemicals, and various fine chemicals.
The fluoroine atoms present in 3,4-difluoro nitrobenzene 3 4-difluoronitrobenzene can be easily changed, increasing its utility as a synthetic tool.
Analytical Characterization of 3,4-Difluoro Nitrobenzene
Analytical characterization of chemical 3,4-difluoro nitrobenzene is a crucial step in understanding its physicochemical properties and potential applications. Numerous analytical techniques can be employed to determine the structure, purity, and properties of this compound. Commonly used methods include {nuclear magnetic resonance (NMR) spectroscopy|ultraviolet-visible (UV-Vis) spectroscopy, which provide information about its arrangement and functional groups. , Furthermore, Moreover , techniques such as gas chromatography-mass spectrometry (GC-MS) or high-performance liquid chromatography-mass spectrometry (HPLC-MS) can be used to quantify the level of 3,4-difluoro nitrobenzene in a mixture.
Via these analytical techniques, we can gain valuable understanding about the properties and behavior of this compound, which is essential for its safe and effective use.
Safety Considerations for Handling 3,4-Difluoro Nitrobenzene
When manipulating 3,4-difluoro nitrobenzene, strict safety protocols are vital. This compound can be dangerous if ingested. Always wear appropriate personal protective apparel, including hand protection, a respirator, and eye protection. Conduct operations in a well-ventilated room and avoid exposure with skin, eyes, and clothing. In case of accidents, follow established procedures for cleanup.
- Retain 3,4-difluoro nitrobenzene in a regulated location away from reactive materials.
- Discard of waste properly according to regional regulations.
- Consult the material safety data sheet (MSDS) for detailed 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 chemical structure consists of a benzene ring modified 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 synthesis of various pharmaceuticals.
Applications of 3,4-Difluoro Nitrobenzene in Pharmaceutical Research
3,4-Difluoro nitrobenzene functions as a versatile building block within the realm of pharmaceutical development. Due to its unique structural properties, such benzene derivative has emerged as a key element in the synthesis of various medicinal agents. Researchers are increasingly harnessing its potential in the design of drugs targeting a wide range of conditions.
One notable application lies in the field of germicidal agents, where 3,4-difluoro nitrobenzene derivatives have demonstrated significant activity against a variety of pathogenic bacteria. Furthermore, its potential in the treatment of allergic disorders is currently investigated.
The chemical versatility of 3,4-difluoro nitrobenzene allows for various modifications and additions, enabling the creation of novel compounds with tailored properties. This adaptability makes it a valuable resource in the ongoing quest to discover effective and non-toxic pharmaceuticals.