• 1. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
• 2. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 3. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 4. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147
• 5. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Diazines Pyrimidines and pyrimidine derivatives Pyrimidinecarboxylic acids and derivatives

Introduction to Methyl-2-Methoxy-4-Methylpyrimidine-5-Carboxylate (CAS No. 198827-04-2)

Methyl-2-methoxy-4-methylpyrimidine-5-carboxylate, identified by its CAS number 198827-04-2, is a significant compound in the realm of chemical and pharmaceutical research. This pyrimidine derivative has garnered attention due to its versatile applications in drug synthesis and molecular biology studies. The compound's unique structural features, including the presence of methoxy and methyl groups, make it a valuable intermediate in the development of various bioactive molecules.

The< strong>2-methoxy and 4-methyl substituents in the pyrimidine core contribute to the compound's reactivity and its potential role in forming complex chemical entities. These functional groups are particularly interesting because they can participate in diverse chemical reactions, such as nucleophilic substitution and condensation reactions, which are crucial for constructing more intricate molecular architectures.

In recent years, there has been a surge in research focused on pyrimidine derivatives due to their broad spectrum of biological activities. Pyrimidines are fundamental building blocks in nucleic acids, and their derivatives have been extensively explored for their pharmacological properties. The< strong>methyl-2-methoxy-4-methylpyrimidine-5-carboxylate compound, with its specific substitution pattern, is being investigated for its potential applications in the development of new therapeutic agents.

One of the most compelling aspects of this compound is its utility as a precursor in the synthesis of heterocyclic compounds. Heterocyclic molecules are known for their diverse biological functions and are widely used in pharmaceuticals. The< strong>carboxylate group in methyl-2-methoxy-4-methylpyrimidine-5-carboxylate provides a reactive site for further functionalization, enabling the creation of more complex structures. This flexibility makes it an attractive candidate for medicinal chemists seeking to design novel drugs.

The< strong>CAS no. 198827-04-2 designation ensures that researchers can reliably identify and procure this compound for their studies. The systematic naming convention provides a clear and unambiguous description of the molecule's structure, which is essential for scientific communication and reproducibility.

Recent advancements in synthetic chemistry have enabled more efficient and scalable production methods for compounds like methyl-2-methoxy-4-methylpyrimidine-5-carboxylate. These improvements have made it possible to conduct larger-scale experiments and screen more compounds for biological activity. The availability of high-quality starting materials is crucial for these endeavors, and this compound fits well within the landscape of readily accessible intermediates.

In addition to its pharmaceutical applications, methyl-2-methoxy-4-methylpyrimidine-5-carboxylate has shown promise in materials science. Pyrimidine derivatives are being explored as components in organic electronic devices due to their electron-deficient nature and ability to form stable conjugated systems. The< strong>methyl and< strong>methoxy groups can influence the electronic properties of the molecule, making it a candidate for use in semiconductors or light-emitting diodes (LEDs).

The compound's stability under various conditions is another area of interest. Researchers are investigating how different storage conditions and reaction environments affect its properties. Understanding these factors is crucial for optimizing synthetic routes and ensuring that the compound remains viable for long-term storage or repeated use in experiments.

The< strong>bioactivity of methyl-2-methoxy-4-methylpyrimidine-5-carboxylate has been a focal point of several recent studies. Researchers have been screening derivatives of this compound for their potential effects on various biological pathways. Some preliminary findings suggest that certain modifications might lead to compounds with anti-inflammatory or anticancer properties.

The development of new synthetic methodologies has also been a key focus area. Researchers are continually seeking ways to improve the efficiency and sustainability of chemical synthesis. The use of< strong>methyl-2-methoxy-4-methylpyrimidine-5-carboxylate as an intermediate exemplifies how traditional heterocyclic chemistry can be adapted to modern needs.

In conclusion, methyl-2-methoxy-4-methylpyrimidine-5-carboxylate(CAS No.198827-04-2) is a multifaceted compound with significant potential in both pharmaceuticals and materials science. Its unique structural features make it a valuable tool for researchers exploring new synthetic pathways and biological applications. As our understanding of its properties continues to grow, so too will its utility in advancing scientific discovery.

• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)