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Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate (CAS No. 117330-40-2): A Comprehensive Overview

Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate, identified by its CAS number CAS No. 117330-40-2, is a sophisticated organic compound that has garnered significant attention in the field of chemical biology and pharmaceutical research. This compound belongs to the bipyridine family, a class of heterocyclic compounds characterized by a pair of adjacent pyridine rings. The presence of dimethyl groups at the 6-position and carboxylate groups at the 4-position enhances its structural complexity and functional versatility, making it a valuable candidate for various applications in medicinal chemistry and material science.

The< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate molecule exhibits unique electronic and steric properties due to its rigid bipyridine core and the electron-withdrawing nature of the carboxylate groups. These characteristics make it an attractive scaffold for designing novel coordination complexes with transition metals. Such complexes have been extensively studied for their potential applications in catalysis, luminescence, and as therapeutic agents.

In recent years, the< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate has been explored for its role in the development of metal-organic frameworks (MOFs). MOFs are porous materials composed of metal ions or clusters connected by organic ligands, offering exceptional surface area and tunable pore sizes. The carboxylate groups in this compound act as effective ligands for metal ions, facilitating the formation of stable and well-defined MOF structures. These MOFs have shown promise in applications such as gas storage, separation technologies, and sensing devices.

Moreover, the< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate has been utilized in the synthesis of functional polymers and supramolecular assemblies. Its ability to form stable complexes with metal ions allows for the creation of polymers with tailored properties. For instance, polymers incorporating this ligand have been shown to exhibit enhanced thermal stability and mechanical strength, making them suitable for advanced materials applications.

The pharmaceutical potential of< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate has also been investigated. Its bipyridine core is known to mimic natural ligands that bind to various biological targets. Researchers have synthesized derivatives of this compound that exhibit inhibitory activity against enzymes involved in cancer progression and infectious diseases. The carboxylate groups provide additional functional handles for further chemical modifications, enabling the development of more potent and selective drug candidates.

In addition to its biological applications, the< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate has been employed in photochemical studies. The bipyridine moiety can act as an antenna system for light absorption, while the carboxylate groups can participate in energy transfer processes. These properties make it a valuable component in the design of photoactive materials such as organic photovoltaics and photocatalysts.

The synthesis of< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4'-dicarboxylate involves multi-step organic reactions that require careful optimization to ensure high yield and purity. Common synthetic routes include condensation reactions between appropriate precursors followed by functional group transformations to introduce the dimethyl and carboxylate groups. Advances in synthetic methodologies have enabled more efficient and scalable production processes for this compound.

The< strong>CAS No. 117330-40-2 identifier is crucial for ensuring consistency and accuracy in scientific literature and patent filings. This unique numerical code distinguishes< strong>Dimethyl 6,6'-dimethyl-[2,2'-bipyridine]-4,4 '-dicarboxylate from other compounds with similar structures or names. The use of CAS numbers facilitates database searches and cross-referencing between different research articles and patents.

The growing interest in< strong>Dimethyl 6 ,6 '- dimeth yl-[2 ,2 '- bipy rid ine ]-4 ,4 '- dicar boxy l ate underscores its importance as a versatile building block in chemical research. Ongoing studies continue to uncover new applications and functionalities for this compound across various disciplines. As our understanding of its properties advances , so too will its impact on innovation in pharmaceuticals , materials science , and beyond.

• 71071-46-0(Dimethyl 2,2'-Bipyridine-4,4'-dicarboxylate)
• 372520-84-8(6,6''-Dimethyl-[2,2':6',2''-terpyridine]-4'-carboxylicacidethylester)
• 797761-32-1(1,3-Benzenedicarboxylic acid, 5-[2-[4-(2-[2,2'-bipyridin]-4-ylethynyl)phenyl]ethynyl]-, 1,3-dimethyl ester)
• 562086-30-0(Methyl 6,6'-dimethyl-[2,2'-bipyridine]-4-carboxylate)
• 330680-46-1(Trimethyl 2,2':6',2''-Terpyridine-4,4',4''-tricarboxylate)
• 1762-42-1(4,4'-Bis(ethoxycarbonyl)-2,2’-bipyridine)
• 797761-34-3(1,3-Benzenedicarboxylic acid,5-[[4-[[4-([2,2'-bipyridin]-4-ylethynyl)phenyl]ethynyl]phenyl]ethynyl]-,dimethyl ester)
• 148332-31-4([2,2':6',2''-Terpyridine]-4'-carboxylicacid, ethyl ester)
• 294211-86-2([2,2':6',2''-Terpyridine]-4'-carboxylicacid, 5,5''-dimethyl-, ethyl ester (9CI))
• 643727-41-7([2,2'-Bipyridine]-5-carboxylic acid, 4'-methyl-, methyl ester)