• 1. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 2. Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer?
  Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
• 3. Emerging 2D hybrid nanomaterials: towards enhanced sensitive and selective conductometric gas sensors at room temperature
  Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
• 4. Establishing the accuracy of position-specific carbon isotope analysis of propane by GC-pyrolysis-GC-IRMS
  ChangjieLiu,PengLiu,XiaofengWang,XiaoqiangLi,JuskeHorita
• 5. Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of arylsulfonyl amides?
  Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330

• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ketones
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Carbonyl compounds Ketones

Comprehensive Guide to 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone (CAS No. 276690-11-0)

1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone (CAS No. 276690-11-0) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, organic synthesis, and material science. This compound, characterized by its unique hydroxy-dimethoxy-methoxymethoxy substitution pattern, serves as a valuable intermediate in the synthesis of complex molecules. Its structural features make it particularly useful in the development of bioactive compounds and advanced materials.

The chemical structure of 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone includes a propanone backbone attached to a phenyl ring substituted with hydroxyl, dimethoxy, and methoxymethoxy groups. This arrangement imparts specific reactivity and solubility properties, making it a versatile building block in synthetic chemistry. Researchers often explore its potential in green chemistry applications, where its derivatization can lead to environmentally friendly processes.

One of the most notable applications of 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone is in the pharmaceutical industry. It serves as a precursor in the synthesis of various drug candidates, particularly those targeting oxidative stress-related diseases and inflammatory conditions. Recent studies have highlighted its role in the development of antioxidant agents, which are increasingly relevant due to rising consumer interest in health and wellness. The compound's ability to modulate reactive oxygen species (ROS) makes it a subject of ongoing research.

In addition to its pharmaceutical applications, 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone is also explored in material science. Its structural motifs are useful in designing advanced polymers and functional coatings. For instance, its incorporation into polymer matrices can enhance thermal stability and mechanical properties, addressing the growing demand for high-performance materials in industries such as automotive and aerospace.

The synthesis of 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone typically involves multi-step organic reactions, including protection and deprotection strategies for the hydroxyl and methoxy groups. Modern synthetic approaches emphasize atom economy and catalytic efficiency, aligning with the principles of sustainable chemistry. Researchers are also investigating enzymatic methods to produce this compound, which could reduce the environmental footprint of its synthesis.

From a commercial perspective, the demand for 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone is driven by its utility in high-value applications. Suppliers and manufacturers are increasingly focusing on custom synthesis and scale-up processes to meet the needs of pharmaceutical and material science clients. The compound's niche market status ensures competitive pricing, but advancements in production technology could make it more accessible in the future.

For researchers and industry professionals, understanding the spectroscopic properties of 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone is crucial. Techniques such as NMR spectroscopy, mass spectrometry, and HPLC analysis are commonly employed to characterize its purity and structural integrity. These analytical methods ensure that the compound meets the stringent quality standards required for its applications.

Looking ahead, the future of 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone lies in its potential for innovation. As the scientific community continues to explore its derivatives and analogs, new applications in drug discovery and smart materials are likely to emerge. Collaboration between academia and industry will be key to unlocking its full potential, particularly in addressing global challenges such as sustainable development and healthcare advancements.

In summary, 1-2-Hydroxy-4,6-dimethoxy-3-(methoxymethoxy)phenyl-1-propanone (CAS No. 276690-11-0) is a multifaceted compound with significant promise across multiple disciplines. Its unique chemical properties, combined with its applications in pharmaceuticals and materials science, make it a subject of enduring interest. As research progresses, this compound is poised to play a pivotal role in the development of next-generation technologies and therapies.

• 18607-90-4(Kakuol)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 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)
• 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)