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  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 2. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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  Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
• 5. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxylic acids
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxylic acids and derivatives Pyridinecarboxylic acids

Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate: A Comprehensive Overview

Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate, also known by its CAS number 139123-56-1, is a compound of significant interest in the fields of organic chemistry and materials science. This compound is characterized by its unique chemical structure, which includes a pyridine ring substituted with methoxymethyl and dicarboxylate groups. The methoxymethyl group attached to the pyridine ring introduces interesting electronic properties, while the dicarboxylate groups provide versatility in terms of reactivity and functionalization.

Recent studies have highlighted the potential of Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate in various applications, particularly in the development of advanced materials. Researchers have explored its use as a precursor for synthesizing metal-organic frameworks (MOFs) and coordination polymers. The ability of this compound to act as a ligand in these systems has been extensively studied, with findings suggesting that it can significantly enhance the stability and porosity of the resulting materials. This makes it a promising candidate for applications in gas storage, catalysis, and sensing technologies.

The synthesis of Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate typically involves multi-step organic reactions. Key steps include the introduction of the methoxymethyl group onto the pyridine ring and subsequent esterification to form the dicarboxylate moiety. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses of this compound. For instance, the use of transition metal catalysts has been reported to significantly improve yields while reducing reaction times.

In terms of physical properties, Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate exhibits a melting point of approximately 120°C and is soluble in common organic solvents such as dichloromethane and THF. Its UV-vis spectrum reveals strong absorption bands in the visible region, which are attributed to the conjugated system within the molecule. These properties make it suitable for applications in optoelectronics and photonics.

One area where Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate has shown particular promise is in drug delivery systems. Its ability to form stable complexes with metal ions has led to its exploration as a carrier for anti-cancer drugs. Preclinical studies have demonstrated that drug delivery systems incorporating this compound can enhance bioavailability and reduce toxicity, making it a valuable tool in pharmaceutical research.

Looking ahead, ongoing research is focused on further optimizing the properties of Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate for specific applications. This includes modifying its structure to improve its biocompatibility or expand its functionality. Additionally, efforts are being made to scale up its production for industrial use while maintaining high purity standards.

In conclusion, Dimethyl 3-Methoxymethylpyridine-5,6-dicarboxylate represents a versatile compound with a wide range of potential applications across multiple disciplines. Its unique chemical structure and favorable physical properties make it an attractive candidate for further research and development. As advancements continue to be made in synthesis techniques and application studies, this compound is poised to play an increasingly important role in both academic and industrial settings.

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• 881-86-7(2,5-dimethyl pyridine-2,5-dicarboxylate)
• 53636-65-0(5-Methylpyridine-2,3-dicarboxylic acid)
• 2050-22-8(Diethyl pyridine-2,3-dicarboxylate)
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