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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Phenylpyrazoles
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Pyrazoles Phenylpyrazoles

2H-Indazole, 2-(4-chlorophenyl)- (CAS No. 61073-53-8): A Comprehensive Overview

2H-Indazole, 2-(4-chlorophenyl)- (CAS No. 61073-53-8) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This heterocyclic compound, featuring an indazole core substituted with a 4-chlorophenyl group, is widely studied for its potential applications in drug discovery and material science. Researchers and industry professionals frequently search for terms like "2H-Indazole derivatives", "chlorophenyl-substituted indazoles", and "CAS 61073-53-8 applications", reflecting the growing interest in this compound.

The molecular structure of 2-(4-chlorophenyl)-2H-indazole consists of a fused benzene and pyrazole ring system, which is a common scaffold in medicinal chemistry. The presence of the chlorophenyl moiety enhances its electronic properties, making it valuable for designing bioactive molecules. Recent trends in AI-driven drug discovery have highlighted the importance of such heterocycles, with searches like "AI in indazole-based drug design" and "computational screening of indazole derivatives" becoming increasingly popular.

One of the key applications of 2H-Indazole, 2-(4-chlorophenyl)- lies in its role as a building block for pharmaceuticals. The compound's structural features make it a promising candidate for developing kinase inhibitors and anti-inflammatory agents. Industry reports and scientific literature often discuss topics such as "indazole-based kinase inhibitors" and "chlorophenyl indazoles in drug development", aligning with current research priorities in targeted therapies.

From a synthetic chemistry perspective, CAS 61073-53-8 serves as an important intermediate in organic synthesis. Its reactivity patterns are frequently explored in studies focusing on "C-H functionalization of indazoles" and "palladium-catalyzed coupling reactions". These areas represent hot topics in modern synthetic methodology, as evidenced by the rising number of publications and patent applications.

The physicochemical properties of 2-(4-chlorophenyl)-2H-indazole contribute to its versatility. With moderate lipophilicity and good stability under various conditions, this compound is suitable for diverse applications. Researchers often investigate parameters like "solubility of chlorophenyl indazoles" and "crystallization behavior of CAS 61073-53-8", which are critical for formulation development.

In material science, 2H-Indazole, 2-(4-chlorophenyl)- has shown potential as a component in organic electronic materials. The conjugated system and electron-withdrawing chlorine atom make it interesting for studies on "organic semiconductors" and "molecular electronics". These applications align with the global push toward sustainable and energy-efficient technologies.

Quality control and analytical characterization of 61073-53-8 are essential aspects for researchers and manufacturers. Common analytical techniques include HPLC purity analysis, mass spectrometry, and NMR spectroscopy. The search terms "analytical methods for indazole derivatives" and "characterization of chlorophenyl-substituted heterocycles" reflect the importance of these quality assurance measures.

The market for 2H-Indazole, 2-(4-chlorophenyl)- has been steadily growing, driven by increasing research activities in pharmaceutical and chemical industries. Market analysts often track keywords like "indazole derivatives market trends" and "demand for chlorophenyl heterocycles" to understand the commercial landscape. The compound's availability from specialized chemical suppliers ensures its accessibility for research purposes.

Safety considerations for handling 2-(4-chlorophenyl)-2H-indazole follow standard laboratory protocols for organic compounds. While not classified as hazardous under normal conditions, proper personal protective equipment and ventilation are recommended. Researchers frequently search for "safety data for CAS 61073-53-8" and "handling procedures for indazole derivatives" to ensure safe laboratory practices.

Future research directions for 2H-Indazole, 2-(4-chlorophenyl)- may include exploring its biological activities more extensively and developing more efficient synthetic routes. The scientific community shows particular interest in "structure-activity relationships of indazole analogs" and "green chemistry approaches to indazole synthesis", indicating potential areas for innovation.

In conclusion, 2H-Indazole, 2-(4-chlorophenyl)- (CAS No. 61073-53-8) represents a valuable chemical entity with diverse applications in pharmaceuticals, materials science, and chemical synthesis. Its unique structural features and growing research interest position it as an important compound in modern chemistry. The continued exploration of its properties and applications will likely yield significant scientific and technological advancements in the coming years.

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