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  Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
• 2. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Bipyridines and oligopyridines

4-Methyl-3,3'-bipyridine: A Comprehensive Overview

4-Methyl-3,3'-bipyridine, also known by its CAS number CAS No 38840-06-1, is a versatile organic compound that has garnered significant attention in various fields of chemistry and materials science. This compound belongs to the family of bipyridines, which are known for their unique electronic properties and wide-ranging applications. In recent years, advancements in synthetic methodologies and computational modeling have further enhanced our understanding of its structure-function relationships, making it a focal point in both academic and industrial research.

The molecular structure of 4-Methyl-3,3'-bipyridine consists of two pyridine rings connected by a single bond at the 3-position of each ring, with a methyl group attached to the 4-position of one of the pyridine rings. This substitution pattern imparts distinctive electronic characteristics, including increased electron-donating ability due to the methyl group. Such features make it an ideal candidate for applications in coordination chemistry, where it can act as a ligand to transition metals, forming stable metal complexes with potential catalytic activity.

Recent studies have highlighted the role of 4-Methyl-3,3'-bipyridine in the development of novel materials for energy storage and conversion. For instance, researchers have explored its use as an organic precursor for synthesizing metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), which exhibit high surface area and porosity. These materials hold promise for applications in gas storage, catalysis, and sensing technologies. The ability of 4-Methyl-3,3'-bipyridine to form robust frameworks stems from its ability to engage in multiple coordination bonds with metal ions, thereby facilitating the construction of hierarchical architectures.

In the realm of electrochemistry, 4-Methyl-3,3'-bipyridine has been investigated as an additive in lithium-ion batteries. Its electron-donating methyl group enhances the redox activity of electrode materials, potentially improving battery performance. Experimental results from recent studies demonstrate that incorporating 4-Methyl-3,3'-bipyridine-derived compounds into cathode materials can lead to higher energy density and better cycling stability compared to conventional materials.

The synthesis of 4-Methyl-3,3'-bipyridine has also seen innovations in recent years. Traditional methods often involved multi-step reactions with low yields; however, modern approaches leveraging microwave-assisted synthesis and continuous flow reactors have significantly improved both efficiency and scalability. These advancements are crucial for meeting the growing demand for this compound in various industries.

Beyond its chemical applications, 4-Methyl-3,3'-bipyridine has found niche uses in pharmaceutical research. Its ability to coordinate with metal ions makes it a potential candidate for designing drug delivery systems or contrast agents for medical imaging. Early-stage studies suggest that metal complexes derived from this compound could exhibit selective binding to certain biological targets without significant toxicity profiles.

In summary, 4-Methyl-3,3'-bipyridine, with its unique structural features and versatile reactivity, continues to be a subject of intense research across multiple disciplines. From energy storage technologies to advanced materials science and pharmaceutical applications, this compound exemplifies how subtle structural modifications can lead to significant functional enhancements. As research progresses and new synthetic strategies emerge, the potential applications of CAS No 38840-06-1-based compounds are expected to expand further.

• 5216-04-6(Pyridine, 3,4-diphenyl-)
• 19352-29-5(4-Methyl-3-phenylpyridine)
• 4479-73-6(3,3'-Dimethyl-4,4'-bipyridine)
• 71523-09-6(3,4'-Bipyridine, 3',5'-dimethyl-)
• 75601-34-2(3-Mesitylpyridine)
• 2052-92-8(Pyridine,3-methyl-4-phenyl-)
• 100004-72-6(Pyridine, 4-methyl-3-(3-methylphenyl)-)
• 112321-80-9(Pyridine, 3,4,5-triphenyl-)
• 780738-75-2(Pyridine, 3-(2,3-dimethylphenyl)-)
• 90395-49-6(Pyridine, 3-(2-methylphenyl)-)