• 1. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Enantio- & chemo-selective preparation of enantiomerically enriched aliphatic nitro alcohols using Candida parapsilosis ATCC 7330
  Sowmyalakshmi Venkataraman RSC Adv., 2015,5, 73807-73813
• 3. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 4. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
• 5. Evolutionary approaches in protein engineering towards biomaterial construction
  Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734

Comprehensive Overview of 4-Oxazolemethanamine,2-(2-methoxyphenyl)- (CAS No. 885274-29-3)

The compound 4-Oxazolemethanamine,2-(2-methoxyphenyl)- (CAS No. 885274-29-3) is a specialized organic molecule that has garnered significant attention in pharmaceutical and agrochemical research. With its unique structural features, this compound serves as a key intermediate in the synthesis of bioactive molecules. Researchers are increasingly exploring its potential applications in drug discovery, particularly in targeting neurological and metabolic disorders, which aligns with current trends in personalized medicine and precision therapeutics.

One of the most searched questions related to 4-Oxazolemethanamine,2-(2-methoxyphenyl)- revolves around its synthetic pathways and mechanism of action. The compound's oxazole core, combined with the methoxyphenyl substituent, offers a versatile scaffold for modifications, making it a valuable building block in medicinal chemistry. Recent studies highlight its role in modulating specific enzyme activities, which could pave the way for novel treatments for conditions like diabetes and inflammation—topics highly relevant to today's health-conscious audience.

From an industrial perspective, CAS No. 885274-29-3 is often discussed in the context of green chemistry and sustainable synthesis. As environmental concerns dominate global discourse, researchers are optimizing its production to minimize waste and energy consumption. This aligns with the growing demand for eco-friendly chemical processes, a hot topic in both academic and industrial circles.

The pharmacokinetic properties of 4-Oxazolemethanamine,2-(2-methoxyphenyl)- are another area of intense investigation. Its bioavailability and metabolic stability are critical factors for its potential use in drug formulations. Given the rise of AI-driven drug design, computational studies on this compound have surged, addressing common queries about its ADME (Absorption, Distribution, Metabolism, and Excretion) profile. Such insights are invaluable for researchers leveraging machine learning to accelerate drug development.

In addition to its pharmaceutical applications, 2-(2-methoxyphenyl)-4-oxazolemethanamine is being explored in material science. Its aromatic and heterocyclic structure contributes to the development of advanced polymers and coatings, which are essential for industries ranging from electronics to automotive. This multidisciplinary relevance makes it a frequent subject in patent filings and R&D reports.

Safety and regulatory compliance are also prominent themes in discussions about CAS No. 885274-29-3. While the compound is not classified as hazardous, proper handling protocols are emphasized to ensure workplace safety—a concern echoed in many online forums and regulatory guidelines. This reflects broader societal shifts toward responsible chemical management.

In summary, 4-Oxazolemethanamine,2-(2-methoxyphenyl)- exemplifies the intersection of innovation and practicality in modern chemistry. Its diverse applications, from life sciences to materials engineering, coupled with its alignment with sustainability goals, ensure its continued relevance in both research and industry. As scientific advancements unfold, this compound is poised to remain a focal point for cutting-edge discoveries.

• 33105-96-3(4-Oxazolemethanamine,2-(4-methylphenyl)-, hydrochloride (1:1))
• 408352-90-9(1-(2-Phenyl-1,3-oxazol-4-yl)methanamine)
• 885273-21-2(2-M-TOLYL-OXAZOL-4-YL-METHYLAMINE)
• 885273-96-1(4-Oxazolemethanol,2-(2-methoxyphenyl)-)
• 885273-44-9(2-(4-Phenylmethoxyphenyl)-1,3-Oxazol-4-YlMethanamine)
• 33105-95-2((2-phenyl-1,3-oxazol-4-yl)methylamine hydrochloride)
• 885273-48-3(4-Oxazolemethanamine,2-(1,3-benzodioxol-5-yl)-)
• 885274-27-1(2-(2-methoxyphenyl)-1,3-oxazole-4-carbaldehyde)
• 885273-17-6(2-(3-methoxyphenyl)-1,3-oxazol-4-ylmethanamine)
• 885272-87-7(C-2-(4-Methoxyphenyl)oxazol-4-ylmethylamine)