3,4-Difluoro Nitrobenzene: Properties and Applications
3,4-Difluoro nitrobenzene acts as an organic compound with the formula C6H3F2NO2. It exists as a white crystal and exhibits a distinct odor. This compound gains applications in the manufacture of diverse bioactive compounds, pesticides, and additional industrial processes.
- On account of its special chemical properties, 3,4-difluoro nitrobenzene acts as a essential precursor in organic synthesis.
- Additionally, its potential for reaction with other molecules permits the synthesis of sophisticated molecular assemblies.
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 exposure of 1,2-difluorobenzene with a mixture of nitric acid and sulfuric acid under carefully controlled temperature. This reaction yields 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 adjusted to enhance the yield and purity of the final product.
- Safety should always be taken when handling nitric acid and sulfuric acid, as these are corrosive substances.
CAS Identifier 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 finds application in various fields, including pharmaceutical synthesis. 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-Difluoro Nitro Benzene: A Chemical Foundation
3,4-Difluoronitrobenzene functions as a crucial precursor in the manufacture of numerous substances. Its unique features make it exceptionally useful for a vast array of applications in sectors such as pharmaceuticals. The structure's presence of both fluorine and nitro groups influences its effectiveness, making it a potent tool for chemists.
- Research into the deployment of 3,4-difluoronitrobenzene are persistent.
- Scientists are constantly investigating innovative ways to harness its capabilities in the development of innovative products.
Analyzing the Hazards of 3,4-Difluoro Nitrobenzene on Environment and Health
3,4-Difluoro nitrobenzene presents itself as an organic compound with potential risks to both human health and the environment. Possesses a varied chemical structure that contributes to its adverse effects. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, 3 4 difluoronitrobenzene cas no leading to a range of symptoms. The ecological impact of this compound contributes to a depletion in biodiversity and impairment of ecosystem functions. The long lifespan of this compound warrants attention to long-term influence on the environment.
- Investigations are ongoing to fully understand the toxicity posed by 3,4-Difluoro nitrobenzene and to develop effective strategies for its mitigation.
- Policies are also under development to restrict the use of this compound and to ensure environmental safety.
Structural Analysis of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a unique arrangement of atoms. Its core is defined by a benzene ring that serves 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 located at a specific location on the ring, significantly influencing the molecule's reactivity. 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.