• 1. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 3. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 4. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?
  Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
• 5. 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

Pyridine, 3-(2-methylphenyl)- (CAS No. 90395-49-6): A Comprehensive Overview

Pyridine, 3-(2-methylphenyl)-, also known by its CAS number 90395-49-6, is a significant compound in the field of organic chemistry. This compound belongs to the class of pyridine derivatives, which are widely studied for their unique chemical properties and applications in various industries. The structure of Pyridine, 3-(2-methylphenyl)- consists of a pyridine ring substituted with a methylphenyl group at the 3-position. This substitution pattern imparts distinct electronic and steric properties to the molecule, making it a valuable intermediate in the synthesis of more complex organic compounds.

Recent advancements in synthetic methodologies have enhanced the efficiency and sustainability of producing Pyridine, 3-(2-methylphenyl)-. Researchers have explored various catalytic systems and reaction conditions to optimize its synthesis. For instance, the use of palladium-catalyzed coupling reactions has been reported as an effective strategy for constructing the carbon-nitrogen bond in this compound. These methods not only improve yield but also reduce environmental impact, aligning with the growing demand for green chemistry practices.

The chemical properties of Pyridine, 3-(2-methylphenyl)- make it an attractive candidate for applications in pharmaceuticals, agrochemicals, and materials science. In the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of bioactive molecules. Its ability to act as a chelating agent or a hydrogen bond donor/acceptor facilitates interactions with biological targets, making it valuable in drug design.

In materials science, Pyridine, 3-(2-methylphenyl)- has been utilized as a building block for constructing functional polymers and coordination polymers. Its nitrogen-containing aromatic ring can coordinate with metal ions, enabling the formation of metal-organic frameworks (MOFs) with potential applications in gas storage and catalysis. Recent studies have demonstrated its role in creating MOFs with high surface area and tunable pore sizes, which are highly sought after in industrial catalysis and separation processes.

The physical properties of Pyridine, 3-(2-methylphenyl)- also contribute to its versatility. It exhibits good solubility in organic solvents such as dichloromethane and acetonitrile, making it suitable for solution-based reactions. Additionally, its thermal stability allows it to be used under moderate heating conditions without decomposition.

From an environmental perspective, understanding the fate and behavior of Pyridine, 3-(2-methylphenyl)- is crucial for assessing its potential impact on ecosystems. Recent studies have focused on its biodegradation pathways under aerobic and anaerobic conditions. These investigations reveal that while the compound is relatively stable under ambient conditions, specific microbial communities can metabolize it into less toxic byproducts.

In conclusion, Pyridine, 3-(2-methylphenyl)- (CAS No. 90395-49-6) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical structure enables its use as an intermediate in drug discovery and materials synthesis while ongoing research continues to uncover new avenues for its utilization. As advancements in synthetic methods and material science progress, this compound is poised to play an even more significant role in driving innovation across various industries.

• 157402-43-2(Pyridine, 3-(2,6-dimethylphenyl)-)
• 5216-04-6(Pyridine, 3,4-diphenyl-)
• 19352-29-5(4-Methyl-3-phenylpyridine)
• 71523-09-6(3,4'-Bipyridine, 3',5'-dimethyl-)
• 75601-34-2(3-Mesitylpyridine)
• 717105-83-4(PYRIDINE, 3,5-BIS(5',6'-DIPHENYL[1,1':2',1''-TERPHENYL]-3'-YL)-)
• 488856-74-2(Pyridine, 3-(2-methylphenyl)-, hydrochloride (1:1))
• 100004-72-6(Pyridine, 4-methyl-3-(3-methylphenyl)-)
• 112321-80-9(Pyridine, 3,4,5-triphenyl-)
• 780738-75-2(Pyridine, 3-(2,3-dimethylphenyl)-)