3,4-Difluoro nitrobenzene is a an organic compound with the formula C6H3F2NO2. It presides as click here a pale yellow crystal and possesses a pronounced odor. This molecule finds applications in the manufacture of numerous pharmaceuticals, agrochemicals, and further commercial processes.
- Due to its distinct chemical properties, 3,4-difluoro nitrobenzene acts as a critical building block in molecular construction.
- Additionally, its potential for reaction with other compounds permits the development of elaborate molecular assemblies.
Synthesis of 3,4-Difluoro Nitrobenzene
The formation 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 temperature. 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 conditions for this reaction can be adjusted 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.
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 1097-26-9. 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 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 production of numerous compounds. Its unique chemical properties make it exceptionally useful for a vast array of applications in industries such as agriculture. The structure's presence 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 continuous.
- Efforts are constantly exploring novel ways to utilize 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 risks 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 ingestion, leading to a range of symptoms. Environmental contamination can result from a depletion in biodiversity and disruption of ecosystem functions. The persistent nature of this compound warrants attention to long-term influence on the environment.
- Investigations are ongoing to better comprehend the hazards posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its mitigation.
- Policies are also being implemented to limit the production of this compound and to ensure environmental safety.
Examination of the Structure of 3,4-Difluoro Nitrobenzene
The molecule of 3,4-difluoro nitrobenzene presents a complex configuration 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 charge distribution. Furthermore, a nitro group (-NO2) is located 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 properties of 3,4-difluoro nitrobenzene.