3,4-Difluoro nitrobenzene is a an chemical compound with the structural representation C6H3F2NO2. It occurs as a pale yellow substance and possesses a distinct odor. This molecule finds applications in the manufacture of diverse bioactive compounds, agrochemicals, and additional industrial processes.
- On account of its unique chemical properties, 3,4-difluoro nitrobenzene acts as a essential building block in chemical reactions.
- Moreover, its reactivity with other molecules allows the development of sophisticated chemical arrangements.
Synthesis of 3,4-Difluoro Nitrobenzene
The preparation 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 reaction 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 separation of the desired product can be achieved through techniques such as recrystallization or distillation.
- The specific conditions for this reaction can be optimized to improve 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.
CAS 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 has a variety of uses 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 acts as a crucial precursor in the synthesis of various chemicals. Its special features make it extremely relevant for a broad spectrum of applications in industries such as pharmaceuticals. The molecule's incorporation of both fluorine and nitro groups enhances its potency, making it a powerful tool for chemists.
- Research into the utilization of 3,4-difluoronitrobenzene are continuous.
- Researchers are constantly exploring creative ways to utilize its capabilities in the development of advanced technologies.
Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene acts as an organic compound with potential threats to both human health and the environment. Possesses a complex chemical structure that contributes to its harmfulness. Exposure to 3,4-Difluoro nitrobenzene can occur through skin contact, leading to diverse adverse reactions. Pollution caused by 3,4-Difluoro nitrobenzene can result from a depletion in biodiversity and damage of ecosystem processes. The stability of this compound raises concerns about its long-term impacts to the environment.
- Research are ongoing to gain a deeper insight into the threats posed by 3,4-Difluoro nitrobenzene and to develop effective strategies for its control.
- Policies are also under development to restrict the production of this compound and to protect human health.
Structural Analysis of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a complex structure 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 polarity. Furthermore, a nitro group (-NO2) is located at a specific location on the ring, significantly influencing here the molecule's interactions. Exploring the spatial arrangement of these functional groups and their effects on each other is crucial for comprehending the overall behavior of 3,4-difluoro nitrobenzene.
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