3,4-Difluoro nitrobenzene serves as an organic compound with the structural representation C₆H₃F₂NO₂. It occurs as a colorless solid and displays a pronounced here odor. This compound finds applications in the synthesis of various pharmaceuticals, agrochemicals, and other commercial applications.

• Because of its special characteristics, 3,4-difluoro nitrobenzene acts as a valuable intermediate in molecular construction.
• Moreover, its potential for reaction with various compounds enables the synthesis of complex organic structures.

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 treatment of 1,2-difluorobenzene with a mixture of nitric acid and sulfuric acid under carefully controlled settings. This reaction 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 parameters for this reaction can be optimized 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 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 1097-25-8. 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 is utilized 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-Difluoronitrobenzene: A Chemical Building Block

3,4-Difluoronitrobenzene acts as a crucial intermediate in the synthesis of various chemicals. Its unique chemical properties make it exceptionally useful for a broad spectrum of applications in industries such as materials science. The compound's inclusion of both fluorine and nitro groups enhances its reactivity, making it a strong tool for chemists.

• Research into the utilization of 3,4-difluoronitrobenzene are persistent.
• Efforts are constantly exploring creative ways to utilize its potential in the development of new technologies.

The Toxic Effects and Ecological Footprint of 3,4-Difluoro Nitrobenzene

3,4-Difluoro nitrobenzene presents itself as an organic compound with potential threats to both human health and the environment. Possesses a complex chemical structure that contributes to its toxicity. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to a range of health issues. The ecological impact of this compound contributes to a degradation in biodiversity and impairment of ecosystem services. The persistent nature of this compound highlights the potential for long-term influence on the environment.

• Research are ongoing to gain a deeper insight into the toxicity posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its control.
• Guidelines are also under development to reduce the use of this compound and to protect human health.

Structural Analysis of 3,4-Difluoro Nitrobenzene

The molecule of 3,4-difluoro nitrobenzene presents a unique arrangement 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 electronegativity. Furthermore, a nitro group (-NO2) is positioned at a specific location on the ring, significantly influencing the molecule's chemical properties. Exploring the spatial arrangement of these functional groups and their influence on each other is crucial for comprehending the overall behavior of 3,4-difluoro nitrobenzene.