3,4-Difluoro nitrobenzene acts as an synthesized molecule with the formula C6H3F2NO2. It presides as a white solid and possesses a characteristic odor. This molecule finds applications in the production of various medicinal drugs, pesticides, and additional industrial applications.
- On account of its special chemical properties, 3,4-difluoro nitrobenzene acts as a valuable precursor in molecular construction.
- Moreover, its potential for reaction with various molecules permits the synthesis of sophisticated molecular assemblies.
Synthesis of 3,4-Difluoro Nitrobenzene
The formation of 3,4-difluoro nitrobenzene is a multi-step process involving the introduction of a nitro group to a pre-existing difluorobenzene structure. One common method involves the reaction of 1,2-difluorobenzene with a mixture of nitric acid and sulfuric acid under carefully controlled temperature. This reaction produces 3,4-difluoro nitrobenzene as the major product. The isolation of the desired product can be achieved through techniques such as recrystallization or distillation.
- The specific conditions for this reaction can be modified to increase the yield and purity of the final product.
- Cautions should always be taken when handling nitric acid and sulfuric acid, as these are reactive substances.
Chemical Abstracts Service Registry Number for 3,4-Difluoro Nitrobenzene: Identification and Usage
The CAS Number is a unique identifier assigned to every chemical compound. For 3,4-Difluoro Nitrobenzene, this number is 1097-26-9. This specific designation is crucial in scientific research, industrial applications, and regulatory contexts. It allows for unambiguous communication and retrieval of information related to this chemical compound. 3,4-Difluoro Nitrobenzene finds application in various fields, including materials science. Its unique structure and properties make it a key intermediate in these applications. Understanding the CAS Number and its significance is therefore fundamental for anyone working with 3,4-Difluoro Nitrobenzene.
3,4-DFNB: A Chemical Construct
3,4-Difluoronitrobenzene functions as a crucial intermediate in the synthesis of diverse substances. Its distinct characteristics make it highly valuable for a wide range of applications in industries such as pharmaceuticals. The compound's presence of both fluorine and nitro groups enhances its potency, making it a potent tool for chemists.
- Research into the application of 3,4-difluoronitrobenzene are ongoing.
- Scientists are constantly investigating innovative ways to utilize its capabilities in the development of advanced technologies.
Analyzing the Hazards of 3,4-Difluoro Nitrobenzene on Environment and Health
3,4-Difluoro nitrobenzene acts as an organic compound with potential threats to both human health and the environment. This chemical exhibits a varied chemical structure that contributes to its harmfulness. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to diverse symptoms. Environmental contamination may lead to a decline in biodiversity and impairment of ecosystem services. The persistent nature of this compound raises concerns about its long-term effects on the environment.
- Investigations are ongoing to fully understand the hazards posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its reduction.
- Policies are also under development to limit the production of this compound and to safeguard the environment.
Structural Analysis of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a complex configuration of atoms. 3 Its core is featured with a benzene ring which acts as the primary scaffold. Attached to this ring are two fluorine atoms at positions 3 and 4, contributing to its polarity. Furthermore, a nitro group (-NO2) is located at a specific location on the ring, significantly influencing the molecule's interactions. Analyzing the spatial arrangement of these functional groups and their effects on each other is crucial for comprehending the overall characteristics of 3,4-difluoro nitrobenzene.