3,4-Difluoro Nitrobenzene: Properties and Applications
3,4-Difluoro nitrobenzene is a an chemical compound with the composition C6H3F2NO2. It exists as a pale yellow solid and displays a pronounced odor. This chemical achieves applications in the production of numerous pharmaceuticals, agrochemicals, and other industrial processes.
- Because of its special traits, 3,4-difluoro nitrobenzene serves as a essential building block in organic synthesis.
- Moreover, its potential for reaction with diverse compounds enables the creation of sophisticated chemical arrangements.
Synthesis of 3,4-Difluoro Nitrobenzene
The formation 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 generates 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 optimized 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 corrosive 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 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-DFNB: A Chemical Construct
3,4-Difluoronitrobenzene acts as a crucial building block in the manufacture of numerous compounds. Its unique chemical properties make it extremely relevant for a broad spectrum of applications in industries such as agriculture. The molecule's inclusion of both fluorine and nitro groups influences its reactivity, making it a strong tool for chemists.
- Research into the application of 3,4-difluoronitrobenzene are continuous.
- Efforts are constantly discovering creative ways to utilize its capabilities in the development of advanced materials.
Analyzing the Hazards of 3,4-Difluoro Nitrobenzene on Environment and Health
3,4-Difluoro nitrobenzene is a an more info organic compound with potential hazards to both human health and the environment. It is a complex chemical structure that contributes to its toxicity. Exposure to 3,4-Difluoro nitrobenzene can occur through inhalation, leading to various adverse reactions. Pollution caused by 3,4-Difluoro nitrobenzene can result from a depletion in biodiversity and disruption of ecosystem functions. The stability of this compound highlights the potential for long-term effects on the environment.
- Investigations are ongoing to fully understand the toxicity posed by 3,4-Difluoro nitrobenzene and to create effective strategies for its mitigation.
- Guidelines are also under development 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 unique configuration of atoms. Its 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 polarity. 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 impact on each other is crucial for comprehending the overall behavior of 3,4-difluoro nitrobenzene.