3,4-Difluoro Nitrobenzene: Properties and Applications
3,4-Difluoro nitrobenzene is a an synthesized molecule with the composition C6H3F2NO2. It occurs as a white solid and displays a pronounced odor. This molecule achieves applications in the manufacture of numerous medicinal drugs, pesticides, and other industrial processes.
- On account of its unique characteristics, 3,4-difluoro nitrobenzene acts as a valuable intermediate in chemical reactions.
- Moreover, its reactivity with diverse molecules enables the creation of elaborate chemical arrangements.
Synthesis of 3,4-Difluoro Nitrobenzene
The synthesis 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 generates 3,4-difluoro nitrobenzene as the major product. The purification of the desired product can be achieved through techniques such as recrystallization or distillation.
- The specific factors for this reaction can be optimized to improve the yield and purity of the final product.
- Precautionary measures 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 1097-27-0. 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 has a variety of uses in various fields, including the production of agrochemicals. 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 precursor in the production of various compounds. Its special chemical properties make it highly valuable for a wide range of applications in fields such as materials science. The molecule's presence of both fluorine and nitro groups influences its potency, making it a strong tool for chemists.
- Research into the deployment of 3,4-difluoronitrobenzene are continuous.
- Efforts are constantly investigating novel ways to utilize its potential in the development of advanced technologies.
Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene presents itself as an organic compound with potential risks to both human health and the environment. This chemical exhibits a multifaceted chemical structure that contributes to its adverse effects. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to various adverse reactions. The ecological impact of this compound may lead to a decline in biodiversity and disruption of ecosystem services. The long lifespan of this compound raises concerns about its long-term influence on the environment.
- Investigations are ongoing to fully understand the threats posed by 3,4-Difluoro nitrobenzene and to create effective strategies for its control.
- Guidelines are also in place to restrict the use of this compound and to protect human health.
Structural Analysis of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents an interesting arrangement of atoms. Its check here core is defined by 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 charge distribution. Furthermore, a nitro group (-NO2) is present at a specific location on the ring, significantly influencing the molecule's interactions. Analyzing the spatial arrangement of these functional groups and their influence on each other is crucial for comprehending the overall behavior of 3,4-difluoro nitrobenzene.