3,4-Difluoro nitrobenzene serves as an organic compound with the formula C₆H₃F₂NO₂. It presides as a colorless crystal and exhibits a distinct odor. This chemical gains applications in the production of various pharmaceuticals, agrochemicals, and further commercial utilization.

• On account of its unique characteristics, 3,4-difluoro nitrobenzene functions as a critical building block in molecular construction.
• Moreover, its potential for reaction with various substances permits the development of elaborate organic structures.

Synthesis of 3,4-Difluoro Nitrobenzene

The formation 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 reaction 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 factors for this reaction can be adjusted to improve the yield and purity of the final product.
• Cautions should always be taken when handling nitric acid and sulfuric acid, as these are dangerous 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 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 functions as a crucial precursor in the synthesis of numerous substances. Its unique characteristics make it extremely relevant for a broad spectrum of applications in fields such as materials science. The compound's inclusion of both fluorine and nitro groups contributes to its reactivity, making it a strong tool for chemists.

• Studies into the application of 3,4-difluoronitrobenzene are ongoing.
• Efforts are constantly investigating creative ways to leverage its features in the development of new materials.

Analyzing the Hazards of 3,4-Difluoro Nitrobenzene on Environment and Health

3,4-Difluoro nitrobenzene acts as an organic compound with potential hazards to both human health and the environment. Possesses a multifaceted chemical structure that contributes to its harmfulness. Exposure to 3,4-Difluoro nitrobenzene can occur through skin contact, leading to a range of symptoms. Environmental contamination can result from a decline in biodiversity and impairment of ecosystem processes. The persistent nature of this compound warrants attention to long-term impacts to the environment.

• Research are ongoing to fully understand the threats posed by 3,4-Difluoro nitrobenzene and to create effective strategies for its mitigation.
• Guidelines are also in place to reduce the use of this compound and to safeguard the environment.

Investigating the Molecular Structure 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 functioning as the primary scaffold. Attached to this ring are two fluorine atoms at positions 3 and 4, contributing to its polarity. Furthermore, a 3 4 difluoronitrobenzene cas no nitro group (-NO2) is located at a specific location on the ring, significantly influencing the molecule's chemical properties. 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.