3,4-Difluoro Nitrobenzene: Properties and Applications

3,4-Difluoro nitrobenzene serves as an organic compound with the structural representation C6H3F2NO2. It presides as a white solid and displays a pronounced odor. This molecule achieves applications in the manufacture of various medicinal drugs, herbicides, and further manufacturing applications.

  • Due to its distinct characteristics, 3,4-difluoro nitrobenzene acts as a critical intermediate in organic synthesis.
  • Additionally, its interaction with diverse substances enables the development of elaborate organic structures.

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 treatment of 1,2-difluorobenzene with a mixture of nitric acid and sulfuric acid under carefully controlled settings. 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 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 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 1097-26-9. This specific designation is crucial in scientific research, industrial applications, and regulatory contexts. It allows for unambiguous communication and retrieval 4-Difluoro Nitrobenzene of information related to this chemical compound. 3,4-Difluoro Nitrobenzene has a variety of uses in various fields, including pharmaceutical synthesis. 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 acts as a crucial building block in the manufacture of numerous substances. Its distinct characteristics make it highly valuable for a broad spectrum of applications in fields such as materials science. The structure's inclusion of both fluorine and nitro groups influences its reactivity, making it a strong tool for chemists.

  • Studies into the utilization of 3,4-difluoronitrobenzene are ongoing.
  • Scientists are constantly discovering novel ways to utilize its capabilities in the development of innovative technologies.

Analyzing the Hazards of 3,4-Difluoro Nitrobenzene on Environment and Health

3,4-Difluoro nitrobenzene acts as an organic compound with potential risks to both human health and the environment. It is a complex chemical structure that contributes to its harmfulness. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to various health issues. Environmental contamination may lead to a decline in biodiversity and disruption of ecosystem functions. The stability of this compound warrants attention to long-term effects on the environment.

  • Studies are ongoing to gain a deeper insight into the threats posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its reduction.
  • Regulations are also in place to restrict the release 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 an interesting configuration of atoms. Its core is featured with 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 polarity. Furthermore, a nitro group (-NO2) is located at a specific location on the ring, significantly influencing the molecule's reactivity. Understanding the spatial arrangement of these functional groups and their effects on each other is crucial for comprehending the overall properties of 3,4-difluoro nitrobenzene.

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