3,4-Difluoro nitrobenzene is a fluorinated benzene derivative with the chemical structure C₆H₃F₂NO₂. It's a pale yellow solid at ambient temperatures. This compound exhibits remarkable traits making it essential for diverse fields.

The creation of 3,4-difluoro nitrobenzene involves a complex procedure. The most common method utilizes fluorination agents to introduce fluorine atoms into the benzene ring. This is followed by a introduction of a nitro group to yield the desired product.

Significant characteristics of 3,4-difluoro nitrobenzene include its high melting point. It also demonstrates moderate reactivity. 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, a highly valuable intermediate, plays an important part in the realm of organic synthesis. Its remarkable composition allows for multiple chemical transformations, making it a flexible building block for synthesizing complex organic compounds.

• Numerous synthetic methodologies have been explored to utilize 3,4-difluoro nitrobenzene in the preparation of numerous target structures.
• , For example , it can be used as a initial reactant for the synthesis of pharmaceuticals, agrochemicals, and numerous fine chemicals.

The fluroine atoms present in 3,4-difluoro nitrobenzene can be easily altered, increasing its utility as a synthetic tool.

Analytical Characterization of 3,4-Difluoro Nitrobenzene

Analytical characterization of compound 3,4-difluoro nitrobenzene is a crucial step in evaluating its physicochemical properties and potential applications. Various analytical techniques can be employed more info to identify the structure, purity, and features of this compound. Commonly used methods include {nuclear magnetic resonance (NMR) spectroscopy|infrared (IR) spectroscopy , which provide information about its composition 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.

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

Safety Considerations for Handling 3,4-Difluoro Nitrobenzene

When manipulating 3,4-difluoro nitrobenzene, strict safety precautions are vital. This material can be toxic if absorbed. Always wear appropriate personal protective gear, including mittens, a respirator, and vision protection. Conduct operations in a well-ventilated room and avoid contact with skin, eyes, and clothing. In case of accidents, follow established protocols for removal.

• Keep 3,4-difluoro nitrobenzene in a tempered 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.

This Chemical Identifier and Molecular Description of 3,4-Difluoro Nitrobenzene

3,4-Difluoro nitrobenzene is a chemical compound with the CAS No. 97975-32-9. Its molecular formula consists of a benzene ring substituted 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 pharmaceuticals.

Applications of 3,4-Difluoro Nitrobenzene in Pharmaceutical Research

3,4-Difluoro nitrobenzene serves a versatile building block within the realm of pharmaceutical investigation. Due to its unique structural properties, such benzene derivative has gained traction as a key element in the formulation of various therapeutic agents. Pharmaceutical experts are increasingly investigating its potential in the development of drugs targeting a broad range of ailments.

One notable application lies in the field of antimicrobial agents, where 3,4-difluoro nitrobenzene compounds have demonstrated remarkable activity against a variety of pathogenic organisms. Furthermore, its potential in the alleviation of allergic disorders is actively investigated.

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