3,4-Difluoro nitrobenzene serves as an chemical compound with the structural representation C6H3F2NO2. It presides as a colorless solid and possesses a pronounced odor. This compound gains applications in the production of numerous pharmaceuticals, herbicides, and further commercial applications.
- On account of its special traits, 3,4-difluoro nitrobenzene functions as a essential building block in chemical reactions.
- Moreover, its interaction with various substances allows the development of complex organic structures.
Synthesis of 3,4-Difluoro Nitrobenzene
The preparation 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 temperature. This reaction generates 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 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 reactive 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 1097-27-0. 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 materials science. 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-DFNB: A Chemical Construct
3,4-Difluoronitrobenzene acts as a crucial intermediate in the manufacture of various chemicals. Its special features make it extremely relevant for a broad spectrum of applications in fields such as pharmaceuticals. The compound's inclusion of both fluorine and nitro groups enhances its potency, making it a potent tool for chemists.
- Investigations into the application of 3,4-difluoronitrobenzene are ongoing.
- Researchers are constantly investigating innovative ways to utilize its features in the development of advanced products.
The Toxic Effects and Ecological Footprint of 3,4-Difluoro Nitrobenzene
3,4-Difluoro nitrobenzene acts here as an organic compound with potential threats to both human health and the environment. Possesses a multifaceted chemical structure that contributes to its toxicity. Exposure to 3,4-Difluoro nitrobenzene can occur through skin contact, leading to various health issues. Environmental contamination may lead to a decline in biodiversity and disruption of ecosystem functions. The long lifespan of this compound warrants attention to long-term influence on the environment.
- Investigations are ongoing to fully understand the threats posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its control.
- Regulations are also being implemented to limit 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 defined by a benzene ring functioning 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 interactions. Understanding 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.