• 1. Excited-state proton-coupled electron transfer within ion pairs?
  Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
• 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. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 4. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147
• 5. 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

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Phenylpyridines

Pyridine, 2-(3-methoxyphenyl)-: A Comprehensive Overview

Pyridine, a heterocyclic aromatic organic compound belonging to the pyridine family, has garnered significant attention in various fields of biomedical research. Among its derivatives, Pyridine, 2-(3-methoxyphenyl)- (CAS No. 4373-58-4) stands out due to its unique chemical structure and potential applications in pharmaceuticals, biochemistry, and materials science.

This compound is characterized by a pyridine ring substituted at the 2-position with a 3-methoxyphenyl group. The presence of the methoxy group at the para position of the phenyl substituent introduces interesting electronic and steric properties, making it a subject of interest for researchers exploring aromatic chemistry and heterocyclic compounds.

The synthesis of Pyridine, 2-(3-methoxyphenyl)- involves several steps, typically starting with the preparation of the phenyl group followed by its coupling with a pyridine derivative. Recent advancements in green chemistry have led to more efficient and environmentally friendly methods for its production, aligning with global efforts towards sustainable chemical manufacturing.

Recent studies have highlighted the potential of this compound in drug discovery. Its unique structure allows it to act as a scaffold for the development of bioactive molecules, including those with antioxidant, anti-inflammatory, and anticancer properties. For instance, research published in Nature Chemistry (2023) demonstrated that derivatives of this compound exhibit promising activity against certain cancer cell lines, making them potential candidates for chemotherapy agents.

Beyond its role in pharmacology, Pyridine, 2-(3-methoxyphenyl)- has also been explored for its applications in biomaterials. Its stability and biocompatibility make it a suitable candidate for use in drug delivery systems, where it can serve as both a carrier and an active ingredient. This dual functionality underscores the versatility of the compound in addressing complex biomedical challenges.

Moreover, advancements in computational chemistry have enabled researchers to predict the behavior of this compound at the molecular level with greater accuracy. Quantum mechanical studies have revealed insights into its electronic transitions and interactions with biological molecules, paving the way for more targeted applications in therapeutic development.

As the field of biomedical engineering continues to evolve, compounds like Pyridine, 2-(3-methoxyphenyl)- are poised to play a crucial role in addressing some of the most pressing health challenges. Ongoing research is focused on optimizing its synthesis, enhancing its bioavailability, and exploring new avenues for its application in diagnostics and therapeutics.

In conclusion, Pyridine, 2-(3-methoxyphenyl)- (CAS No. 4373-58-4) is a multifaceted compound with significant potential in the biomedical sciences. Its unique structure, coupled with recent advancements in its synthesis and application, positions it as a key player in the development of next-generation pharmaceuticals and biomaterials. As research continues to uncover new properties and applications, this compound is likely to remain at the forefront of biomedical innovation.

• 98061-22-4(3-(pyridin-2-yl)phenol)
• 5957-90-4(2-(4-Methoxyphenyl)pyridine)
• 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)