4-Chloro-2-phenylaniline - 73006-78-7

4-Chloro-2-phenylaniline

Catalog Number: EVT-3161535
CAS Number: 73006-78-7
Molecular Formula: C12H10ClN
Molecular Weight: 203.67 g/mol
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Product Introduction

Description
4-Chloro-2-phenylaniline is a chemical compound that belongs to the class of anilines. It is widely used in various fields, including medical, environmental, and industrial research. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, effects on cell function and signal transduction, applications in different research areas, and future perspectives and challenges associated with 4-Chloro-2-phenylaniline.
Applications in Various Fields
In Medical Research, 4-Chloro-2-phenylaniline plays a crucial role in drug development. It has shown promising results in preclinical studies, demonstrating its potential as a therapeutic agent for various diseases, including cancer and neurological disorders. Clinical trials are underway to evaluate its efficacy and safety in humans. However, potential side effects need to be carefully monitored and managed.
In Environmental Research, 4-Chloro-2-phenylaniline's effects on ecosystems and its role in pollution management are being studied. It has been found to have adverse effects on aquatic organisms, highlighting the need for proper disposal and management to minimize environmental impact. Sustainability and environmental considerations are essential in the use and disposal of this compound.
In Industrial Research, 4-Chloro-2-phenylaniline is used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations are crucial to ensure the well-being of workers involved in its production and handling. Proper safety protocols and risk assessments should be implemented to mitigate any potential hazards.

Properties

CAS Number

73006-78-7

Product Name

4-Chloro-2-phenylaniline

IUPAC Name

4-chloro-2-phenylaniline

Molecular Formula

C12H10ClN

Molecular Weight

203.67 g/mol

InChI

InChI=1S/C12H10ClN/c13-10-6-7-12(14)11(8-10)9-4-2-1-3-5-9/h1-8H,14H2

InChI Key

HTPGFCKKCPBMTH-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)C2=C(C=CC(=C2)Cl)N

Canonical SMILES

C1=CC=C(C=C1)C2=C(C=CC(=C2)Cl)N
Method of Synthesis or Extraction
Several methods are commonly used for the synthesis of 4-Chloro-2-phenylaniline. One of the most efficient methods involves the reaction of 4-chloronitrobenzene with aniline in the presence of a catalyst, such as palladium or copper. This method offers a high yield of the desired product. However, it is important to consider environmental and safety considerations during the synthesis process. Proper waste management and adherence to safety protocols are crucial to minimize any potential risks associated with the synthesis of 4-Chloro-2-phenylaniline.
Chemical Structure and Biological Activity
The chemical structure of 4-Chloro-2-phenylaniline consists of a chloro group attached to the fourth carbon atom of a benzene ring, with an amino group attached to the second carbon atom. This compound exhibits significant biological activity due to its interaction with specific biological targets. The mechanism of action involves binding to target proteins, enzymes, or receptors, leading to modulation of cellular processes.
Biological Effects
The effects of 4-Chloro-2-phenylaniline on cell function and signal transduction are diverse. It has been shown to influence various cellular pathways, including cell proliferation, apoptosis, and differentiation. Additionally, this compound can affect signal transduction cascades, leading to altered gene expression and protein synthesis. The potential therapeutic effects of 4-Chloro-2-phenylaniline are being explored in drug development, while its toxic effects are also being investigated to ensure safe usage.
Future Perspectives and Challenges
Despite the potential applications of 4-Chloro-2-phenylaniline, there are current limitations in its use and study. Further research is needed to fully understand its mechanism of action, optimize synthesis methods, and evaluate its long-term effects. Possible solutions and improvements include the development of more sustainable synthesis methods and the identification of specific biological targets for therapeutic applications.
Future trends and prospects in the application of 4-Chloro-2-phenylaniline in scientific research include the exploration of its combination with other compounds for synergistic effects and the development of targeted delivery systems. Additionally, advancements in analytical techniques will enable better characterization and understanding of its biological activity.
In conclusion, 4-Chloro-2-phenylaniline is a versatile compound with significant potential in various research areas. Its synthesis methods, biological activity, effects, and applications have been discussed in this paper. However, further research and careful consideration of environmental and safety aspects are necessary to fully harness its benefits and mitigate any potential risks.

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