3,4-Difluoro nitrobenzene is a an synthesized molecule with the composition C6H3F2NO2. It exists as a pale yellow solid and displays a distinct odor. This molecule gains applications in the production of diverse medicinal drugs, agrochemicals, and additional commercial applications.
- On account of its distinct traits, 3,4-difluoro nitrobenzene acts as a essential building block in chemical reactions.
- Furthermore, its potential for reaction with various compounds permits the development of elaborate molecular assemblies.
Synthesis of 3,4-Difluoro Nitrobenzene
The preparation 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 website produces 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 improve the yield and purity of the final product.
- Safety 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 finds application 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-Difluoro Nitro Benzene: A Chemical Foundation
3,4-Difluoronitrobenzene serves as a crucial building block in the production of numerous chemicals. Its special features make it extremely relevant for a vast array of applications in fields such as agriculture. The structure's inclusion of both fluorine and nitro groups contributes to its effectiveness, making it a strong tool for chemists.
- Research into the deployment of 3,4-difluoronitrobenzene are continuous.
- Researchers are constantly investigating creative ways to harness its potential in the development of advanced materials.
Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene is a an organic compound with potential hazards to both human health and the environment. It is a complex chemical structure that contributes to its adverse effects. Exposure to 3,4-Difluoro nitrobenzene can occur through skin contact, leading to diverse health issues. The ecological impact of this compound contributes to a degradation in biodiversity and disruption of ecosystem processes. The persistent nature of this compound warrants attention to long-term influence on the environment.
- Investigations are ongoing to better comprehend the toxicity posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its control.
- Guidelines are also in place to restrict the use of this compound and to protect human health.
Investigating the Molecular Structure of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a complex configuration 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 positioned 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.