1-Chloro-2-iodo-4-nitrobenzene - 74534-15-9

1-Chloro-2-iodo-4-nitrobenzene

Catalog Number: EVT-3161651
CAS Number: 74534-15-9
Molecular Formula: C6H3ClINO2
Molecular Weight: 283.45 g/mol
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Product Introduction

Description
1-Chloro-2-iodo-4-nitrobenzene is a chemical compound that belongs to the class of halogenated aromatic compounds. It is widely used in various fields, including medical research, environmental research, and industrial applications. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, and applications of 1-Chloro-2-iodo-4-nitrobenzene.
Applications in Various Fields
In Medical Research, 1-Chloro-2-iodo-4-nitrobenzene plays a crucial role in drug development. It is used as a starting material for the synthesis of novel compounds with potential therapeutic properties. Clinical trials have been conducted to evaluate the efficacy and safety of these compounds in various diseases. The benefits of using 1-Chloro-2-iodo-4-nitrobenzene in drug development include its ability to target specific biological pathways and its potential for improved treatment outcomes. However, potential side effects and toxicity profiles need to be thoroughly evaluated during the drug development process.
In Environmental Research, 1-Chloro-2-iodo-4-nitrobenzene is used to study its effects on ecosystems. It is known to have an impact on aquatic organisms and can contribute to pollution in water bodies. Understanding its role in pollution management is crucial for developing sustainable environmental practices. The compound's environmental impact should be carefully assessed to minimize its adverse effects on ecosystems.
In Industrial Research, 1-Chloro-2-iodo-4-nitrobenzene is used in various manufacturing processes. It can be employed as a reagent or intermediate in the synthesis of other chemicals. Its use can improve product quality and efficiency in industries such as pharmaceuticals, agrochemicals, and dyes. Health and safety considerations are of utmost importance in industrial settings to protect workers and prevent environmental contamination.

Properties

CAS Number

74534-15-9

Product Name

1-Chloro-2-iodo-4-nitrobenzene

IUPAC Name

1-chloro-2-iodo-4-nitrobenzene

Molecular Formula

C6H3ClINO2

Molecular Weight

283.45 g/mol

InChI

InChI=1S/C6H3ClINO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H

InChI Key

LOQLBMYYBHCMJJ-UHFFFAOYSA-N

SMILES

C1=CC(=C(C=C1[N+](=O)[O-])I)Cl

Canonical SMILES

C1=CC(=C(C=C1[N+](=O)[O-])I)Cl
Method of Synthesis or Extraction
1-Chloro-2-iodo-4-nitrobenzene can be synthesized through several methods, including the Sandmeyer reaction and the diazotization reaction. The Sandmeyer reaction involves the conversion of an aryl diazonium salt to the corresponding halogenated compound. On the other hand, the diazotization reaction involves the conversion of aniline to the corresponding diazonium salt, followed by halogenation.
The efficiency and yield of each method vary depending on the reaction conditions and the starting materials used. The Sandmeyer reaction generally provides good yields, while the diazotization reaction may require additional steps for purification. Environmental and safety considerations should be taken into account during the synthesis process, as some of the reagents used may be hazardous or toxic. Proper waste disposal and adherence to safety protocols are essential to minimize environmental impact and ensure the safety of the researchers involved.
Chemical Structure and Biological Activity
The chemical structure of 1-Chloro-2-iodo-4-nitrobenzene consists of a benzene ring with chlorine, iodine, and nitro groups attached at specific positions. This unique structure contributes to its biological activity and potency.
The compound exhibits a mechanism of action that involves interaction with specific biological targets. It has been found to inhibit certain enzymes and receptors, leading to various biological effects. The potency of 1-Chloro-2-iodo-4-nitrobenzene varies depending on the target and the concentration used.
Biological Effects
1-Chloro-2-iodo-4-nitrobenzene has been shown to affect cell function and signal transduction pathways. It can modulate cellular processes such as proliferation, differentiation, and apoptosis. The compound's potential therapeutic effects have been investigated in various disease models, including cancer, inflammation, and neurological disorders.
However, it is important to note that 1-Chloro-2-iodo-4-nitrobenzene may also have toxic effects on cells and tissues. High concentrations or prolonged exposure to the compound can lead to cytotoxicity and tissue damage. Careful evaluation of the dose and duration of exposure is necessary to minimize potential toxic effects.
Future Perspectives and Challenges
Despite the potential applications of 1-Chloro-2-iodo-4-nitrobenzene, there are current limitations in its use and study. The compound's stability, solubility, and bioavailability need to be further optimized for better efficacy and safety. Additionally, the development of more efficient synthesis methods and purification techniques is essential to improve yield and reduce environmental impact.
Possible solutions and improvements include the exploration of alternative synthetic routes and the development of novel derivatives with enhanced properties. Future trends and prospects in the application of 1-Chloro-2-iodo-4-nitrobenzene in scientific research include its potential use as a tool compound for target identification and validation, as well as its application in personalized medicine and drug delivery systems.
In conclusion, 1-Chloro-2-iodo-4-nitrobenzene is a versatile compound with significant potential in various fields. Its synthesis methods, chemical structure, biological activity, and applications have been discussed in this paper. Further research and development are needed to overcome current limitations and fully explore the compound's potential in scientific research and industrial applications.

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