3,4-Difluoro nitrobenzene is a an organic compound with the formula C₆H₃F₂NO₂. It exists as a colorless crystal and possesses a pronounced odor. This chemical gains applications in the production of numerous medicinal drugs, pesticides, and further industrial processes.

• Because of its unique traits, 3,4-difluoro nitrobenzene acts as a critical intermediate in molecular construction.
• Additionally, its reactivity with various substances allows the creation of complex molecular assemblies.

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 exposure of 1,2-difluorobenzene with a mixture of nitric acid and sulfuric acid under carefully controlled conditions. 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 parameters 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.

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 1097-27-0. 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 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-DFNB: A Chemical Construct

3,4-Difluoronitrobenzene functions as a crucial building block in the production of numerous compounds. Its special characteristics make it highly valuable for a wide range of applications in fields such as agriculture. The compound's presence of both fluorine and nitro groups influences its potency, making it a strong tool for chemists.

• Studies into the application of 3,4-difluoronitrobenzene are continuous.
• Researchers are constantly exploring innovative ways to harness its potential in the development of new materials.

Toxicity and Environmental Impact of 3,4-Difluoro Nitrobenzene

3,4-Difluoro nitrobenzene presents itself as an click here organic compound with potential hazards to both human health and the environment. It is a multifaceted chemical structure that contributes to its harmfulness. Exposure to 3,4-Difluoro nitrobenzene can occur through ingestion, leading to a range of health issues. The ecological impact of this compound may lead to a decline in biodiversity and impairment of ecosystem processes. The long lifespan of this compound warrants attention to long-term effects on the environment.

• Research are ongoing to gain a deeper insight into the threats posed by 3,4-Difluoro nitrobenzene and to create effective strategies for its mitigation.
• Guidelines are also in place to reduce the production of this compound and to ensure environmental safety.

Structural Analysis of 3,4-Difluoro Nitrobenzene

The molecule of 3,4-difluoro nitrobenzene presents a complex arrangement 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 present at a specific location on the ring, significantly influencing the molecule's chemical properties. Understanding the spatial arrangement of these functional groups and their effects on each other is crucial for comprehending the overall characteristics of 3,4-difluoro nitrobenzene.