3,4-Difluoro nitrobenzene is a an chemical compound with the structural representation C6H3F2NO2. It occurs as a pale yellow solid and displays a characteristic odor. This compound gains applications in the production of various medicinal drugs, agrochemicals, and other commercial utilization.
- Due to its special traits, 3,4-difluoro nitrobenzene serves as a essential building block in chemical reactions.
- Additionally, its interaction with various molecules enables the creation of sophisticated molecular assemblies.
Synthesis of 3,4-Difluoro Nitrobenzene
The formation of 3,4-difluoro nitrobenzene is a multi-step process involving the nitration 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 settings. This reaction yields 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 modified to increase the yield and purity of the final product.
- Precautionary measures 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 1097-25-8. 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 finds application in various fields, including pharmaceutical synthesis. Its unique structure and properties make it an essential component 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 serves as a crucial precursor in the synthesis of diverse substances. Its unique 3 4 difluoronitrobenzene cas no features make it highly valuable for a vast array of applications in fields such as materials science. The molecule's presence of both fluorine and nitro groups enhances its effectiveness, making it a powerful tool for chemists.
- Studies into the deployment of 3,4-difluoronitrobenzene are persistent.
- Efforts are constantly exploring creative ways to harness its features in the development of advanced products.
Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene is a an organic compound with potential threats to both human health and the environment. This chemical exhibits a complex chemical structure that contributes to its toxicity. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to a range of adverse reactions. The ecological impact of this compound can result from a depletion in biodiversity and disruption of ecosystem services. The persistent nature of this compound raises concerns about its long-term influence on the environment.
- Studies are ongoing to better comprehend the threats posed by 3,4-Difluoro nitrobenzene and to develop effective strategies for its reduction.
- Policies are also under development to reduce the production of this compound and to safeguard the environment.
Investigating the Molecular Structure of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a complex structure of atoms. Its core is composed of 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 positioned at a specific location on the ring, significantly influencing the molecule's interactions. Analyzing the spatial arrangement of these functional groups and their impact on each other is crucial for comprehending the overall characteristics of 3,4-difluoro nitrobenzene.