3,4-Difluoro nitrobenzene is a an organic compound with the structural representation C₆H₃F₂NO₂. It exists as a pale yellow substance and displays a distinct odor. This molecule finds applications in the manufacture of numerous bioactive compounds, agrochemicals, and additional manufacturing utilization.

• Because of its special characteristics, 3,4-difluoro nitrobenzene serves as a essential intermediate in organic synthesis.
• Additionally, its potential for reaction with diverse substances enables the creation of sophisticated organic structures.

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 exposure 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 isolation of the desired product can be achieved through techniques such as recrystallization or distillation.

• The specific conditions for this reaction can be adjusted to increase 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.

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 1097-27-0. This specific designation is crucial in scientific research, industrial applications, and regulatory contexts. It allows 3 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 synthesis of diverse chemicals. Its distinct features make it exceptionally useful for a vast array of applications in sectors such as materials science. The structure's inclusion of both fluorine and nitro groups contributes to its potency, making it a powerful tool for chemists.

• Research into the deployment of 3,4-difluoronitrobenzene are persistent.
• Scientists are constantly exploring innovative ways to utilize its potential in the development of innovative materials.

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

3,4-Difluoro nitrobenzene is a an organic compound with potential threats to both human health and the environment. This chemical exhibits a varied chemical structure that contributes to its adverse effects. Exposure to 3,4-Difluoro nitrobenzene can occur through skin contact, leading to diverse symptoms. Environmental contamination can result from a depletion in biodiversity and disruption of ecosystem functions. The stability of this compound highlights the potential for long-term impacts to the environment.

• Investigations are ongoing to gain a deeper insight into the threats posed by 3,4-Difluoro nitrobenzene and to formulate effective strategies for its control.
• Regulations are also in place to reduce the production of this compound and to protect human health.

Investigating the Molecular Structure of 3,4-Difluoro Nitrobenzene

The molecule of 3,4-difluoro nitrobenzene presents a unique configuration of atoms. Its core is composed of a benzene ring functioning 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 interactions. Understanding 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.