3,4-Difluoro Nitrobenzene: Properties and Applications
3,4-Difluoro nitrobenzene acts as an synthesized molecule with the structural representation C6H3F2NO2. It presides as a pale yellow crystal and exhibits a pronounced odor. This chemical gains applications in the manufacture of various pharmaceuticals, agrochemicals, and additional commercial utilization.
- Due to its distinct characteristics, 3,4-difluoro nitrobenzene acts as a essential intermediate in chemical reactions.
- Moreover, its potential for reaction with other compounds enables the synthesis of sophisticated chemical arrangements.
Synthesis of 3,4-Difluoro Nitrobenzene
The synthesis of 3,4-difluoro nitrobenzene is a multi-step process involving the addition of a nitro group to a pre-existing difluorobenzene structure. One common method involves the treatment 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 separation of the desired product can be achieved through techniques such as recrystallization or distillation.
- The specific conditions for this reaction can be modified to enhance 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 click here to every chemical compound. For 3,4-Difluoro Nitrobenzene, this number is 1097-25-8. 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 valuable reagent in these applications. Understanding the CAS Number and its significance is therefore fundamental for anyone working with 3,4-Difluoro Nitrobenzene.
3,4-Difluoronitrobenzene: A Chemical Building Block
3,4-Difluoronitrobenzene functions as a crucial precursor in the synthesis of various compounds. Its unique features make it exceptionally useful for a vast array of applications in industries such as pharmaceuticals. The molecule's inclusion of both fluorine and nitro groups influences its potency, making it a powerful tool for chemists.
- Investigations into the utilization of 3,4-difluoronitrobenzene are persistent.
- Researchers are constantly discovering creative ways to harness its capabilities in the development of new products.
Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene presents itself as an organic compound with potential hazards to both human health and the environment. It is a varied chemical structure that contributes to its adverse effects. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to a range of adverse reactions. Pollution caused by 3,4-Difluoro nitrobenzene contributes to a degradation in biodiversity and disruption of ecosystem processes. 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 formulate effective strategies for its control.
- Policies are also in place to reduce the use of this compound and to ensure environmental safety.
Examination of the Structure of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents an interesting configuration of atoms. Its core is defined by a benzene ring functioning as the primary scaffold. Attached to this ring are two fluorine atoms at positions 3 and 4, contributing to its electronegativity. Furthermore, a nitro group (-NO2) is present at a specific location on the ring, significantly influencing the molecule's reactivity. Analyzing the spatial arrangement of these functional groups and their influence on each other is crucial for comprehending the overall properties of 3,4-difluoro nitrobenzene.