• 1. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 2. Emerging investigator series: first-principles and thermodynamics comparison of compositionally-tuned delafossites: cation release from the (001) surface of complex metal oxides?
  Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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  Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Tertiary amines

Comprehensive Overview of 2-(Dimethylamino)-4-methylpyrimidin-5-ol (CAS No. 92635-40-0)

2-(Dimethylamino)-4-methylpyrimidin-5-ol (CAS No. 92635-40-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This pyrimidine derivative is characterized by its unique molecular structure, featuring a dimethylamino group and a hydroxyl substituent, which contribute to its reactivity and potential applications. The compound’s CAS number 92635-40-0 serves as a critical identifier for researchers and regulatory bodies, ensuring precise communication in scientific literature and commercial transactions.

In recent years, the demand for pyrimidine-based compounds has surged due to their versatility in drug discovery and material science. 2-(Dimethylamino)-4-methylpyrimidin-5-ol is no exception, with studies highlighting its role as a building block for synthesizing more complex molecules. Its structural motifs are often explored in the development of kinase inhibitors and antimicrobial agents, aligning with the growing interest in targeted therapies and antibiotic resistance solutions. Researchers frequently search for "92635-40-0 synthesis" or "2-(Dimethylamino)-4-methylpyrimidin-5-ol applications," reflecting the compound’s relevance in cutting-edge science.

The compound’s physicochemical properties, such as solubility and stability, are critical for its practical use. Analytical techniques like HPLC and NMR spectroscopy are commonly employed to characterize CAS 92635-40-0, ensuring purity and consistency in research settings. Additionally, its molecular weight and logP value are frequently queried by chemists optimizing formulations for bioavailability or environmental compatibility. These metrics are essential for industries prioritizing sustainable and efficient chemical processes.

From an industrial perspective, 2-(Dimethylamino)-4-methylpyrimidin-5-ol is often discussed in the context of green chemistry and process optimization. Companies are increasingly seeking ways to reduce waste and energy consumption during synthesis, making this compound a candidate for innovative catalytic methods. Searches for "eco-friendly pyrimidine synthesis" or "92635-40-0 scalable production" underscore the intersection of economic and environmental priorities in modern chemical manufacturing.

In the realm of intellectual property, patents involving CAS No. 92635-40-0 frequently focus on its derivatives for therapeutic use. For instance, modifications to the dimethylamino group have yielded compounds with enhanced bioactivity, a topic of interest for pharmaceutical developers. This aligns with broader trends in personalized medicine and structure-activity relationship (SAR) studies, where subtle molecular changes can significantly impact efficacy and safety.

Educational resources and databases often highlight 2-(Dimethylamino)-4-methylpyrimidin-5-ol as a case study in heterocyclic chemistry. Its synthesis routes, such as cyclocondensation reactions, are taught in advanced organic chemistry courses, catering to students and professionals alike. Queries like "pyrimidine reaction mechanisms" or "92635-40-0 spectroscopic data" reflect the compound’s didactic value in bridging theoretical knowledge and practical applications.

Looking ahead, the trajectory of CAS 92635-40-0 research is likely to intersect with emerging technologies like AI-driven drug design and automated synthesis platforms. Computational models predicting the compound’s interactions with biological targets could accelerate its adoption in preclinical studies. Furthermore, the rise of open-access chemical databases has made information about 2-(Dimethylamino)-4-methylpyrimidin-5-ol more accessible, fostering collaboration across academia and industry.

In summary, 2-(Dimethylamino)-4-methylpyrimidin-5-ol (CAS No. 92635-40-0) exemplifies the dynamic interplay between fundamental chemistry and applied science. Its multifaceted applications—from pharmaceuticals to sustainable manufacturing—make it a compound of enduring interest. As scientific inquiry evolves, so too will the innovative uses of this pyrimidine derivative, solidifying its place in the lexicon of modern chemistry.

• 107361-61-5(2-(dimethylamino)-4-phenylpyrimidin-5-ol)
• 685897-68-1(2-amino-4,6-dimethylpyrimidin-5-ol)
• 1749-71-9(5-Methoxy-4-methylpyrimidin-2-amine)
• 92635-35-3(5-Pyrimidinol, 2-(ethylamino)-4-methyl-)
• 345642-90-2(2-(dimethylamino)-4,6-dimethylpyrimidin-5-ol)
• 92635-36-4(2-(Hexylamino)-4-methylpyrimidin-5-OL)
• 92635-39-7(5-Pyrimidinol, 4-methyl-2-[(phenylmethyl)amino]-)
• 112934-56-2(5-Pyrimidinol, 2-(dimethylamino)-4-(3-methylphenyl)-)
• 637363-33-8(5-PYRIMIDINOL, 2-(DIMETHYLAMINO)-4,6-BIS(1,1-DIMETHYLETHYL)-)
• 92635-38-6(5-Pyrimidinol, 2-amino-4-methyl- (9CI))