320-60-5 | 2,4-Dichlorobenzotrifluoride

CAS:320-60-5 | 2,4-Dichlorobenzotrifluoride,Description

Synthesis Analysis

The synthesis of 2,4-dichlorobenzotrifluoride involves several chemical reactions, starting from commercially available precursors. An efficient synthesis route for related compounds has been demonstrated through a sequence of nitration, selective reduction, diazotization, and chlorination, yielding high product yields (Wei‐Yi Zhou et al., 2015). This methodology underscores the potential for synthesizing dichlorobenzotrifluoride derivatives efficiently.

Molecular Structure Analysis

The molecular structure of dichlorobenzotrifluorides, including 2,4-dichlorobenzotrifluoride, has been explored through various analytical techniques. Studies on related fluorinated compounds reveal the impact of fluorination on molecular structure, indicating strong Lewis base behavior of fluorine atoms and their interactions with other molecules (K. Christe et al., 1990). These findings help in understanding the structural aspects of 2,4-dichlorobenzotrifluoride.

Chemical Reactions and Properties

2,4-Dichlorobenzotrifluoride undergoes various chemical reactions, showcasing its reactivity and versatility. For example, metalation and derivatization studies on dichlorobenzotrifluorides have shown selective reactivity patterns, indicating the potential for creating diverse chemical structures from 2,4-dichlorobenzotrifluoride (E. Masson et al., 2005).

Physical Properties Analysis

The physical properties of 2,4-dichlorobenzotrifluoride, such as melting and boiling points, solubility, and density, are crucial for its handling and application in various chemical processes. Research on similar fluorinated compounds has provided insights into how fluorination affects the physical properties of aromatic compounds, suggesting that 2,4-dichlorobenzotrifluoride likely possesses unique physical characteristics conducive to specialized applications (H. Yeo et al., 2015).

Chemical Properties Analysis

The chemical properties of 2,4-dichlorobenzotrifluoride, including reactivity with various chemical reagents, stability under different conditions, and its role as a precursor or intermediate in organic syntheses, have been explored. Studies focusing on the reactivity and stability of fluorinated compounds highlight the influence of fluorination on chemical behavior, which is relevant for understanding the chemical properties of 2,4-dichlorobenzotrifluoride (Jonathan T. Lyon & L. Andrews, 2007).

Scientific Research Applications

• Organic Chemistry : It is used in the metalation and derivatization of organometallic intermediates, crucial for synthesizing various compounds (Masson et al., 2005).
• Nanotechnology : 2,4-Dichlorobenzotrifluoride plays a role in the liquid-phase syntheses of inorganic nanoparticles, which are essential in chemical research with broad applications in industry and technology (Cushing, Kolesnichenko, & O'connor, 2004).
• Herbicide Development : As an active ingredient in selective herbicides, it mimics natural auxin, leading to abnormal growth and death in targeted plants (Song, 2014). Its impact on ecosystems and human health is also a significant research area (Islam et al., 2017).
• Toxicity and Environmental Impact : Studies focus on its toxicity, including occupational risk, neurotoxicity, resistance, and impacts on non-target species (Zuanazzi, Ghisi, & Oliveira, 2020). Additionally, the degradation of 2,4-dichlorophenoxyacetic acid in environmental settings is an area of research, aiming to reduce its toxicity and increase biodegradability (Jaafarzadeh, Ghanbari, & Ahmadi, 2017).
• Soil and Microbial Studies : Long-term application of 2,4-D in soil affects microbial populations and biochemical processes, with ester formulations showing more marked effects (Rai, 1992).
• Sensor Technology : Development of highly selective and sensitive sensors for detecting 2,4-D, essential for monitoring environmental pollutants (Shi, Zhao, Liu, & Zhu, 2011).
• Bioremediation : Strategies for removing 2,4-D from contaminated water sources and soils are under investigation, with a focus on developing more efficient and environmentally friendly methods (EvyAliceAbigail, MelvinSamuel, Needhidasan, & Ramalingam, 2017).
• Agricultural Biotechnology : Engineering crops to be resistant to 2,4-D damage is another significant area of research, making them more resilient to herbicide drift (Bayley, Trolinder, Ray, Morgan, Quisenberry, & Ow, 1992).

Safety And Hazards

2,4-Dichlorobenzotrifluoride is a hazardous chemical and should be handled with care. It is toxic, and its vapor has a stimulating effect on the respiratory system. Safety measures include avoiding breathing its dust/fume/gas/mist/vapors/spray, washing face, hands, and any exposed skin thoroughly after handling, wearing protective gloves/clothing/eye protection/face protection, and keeping away from heat/sparks/open flames/hot surfaces.

More Information