• 1. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
• 2. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
  Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
• 3. An atomic scale study of defects in Co2FeAl
  Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
• 4. An intensified π-hole in beryllium-doped boron nitride meshes: its determinant role in CO2 conversion into hydrocarbon fuels?
  Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
• 5. An analysis of the WTC fires using CIB correlations and simple modeling
  JGQuintiere

Comprehensive Overview of 3-Bromo-5-(methoxymethyl)isoxazole (CAS No. 1220521-36-7): Properties, Applications, and Industry Insights

3-Bromo-5-(methoxymethyl)isoxazole (CAS No. 1220521-36-7) is a specialized heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research. This brominated isoxazole derivative features a unique molecular structure, combining a methoxymethyl group with a reactive bromo substituent, making it a versatile intermediate for synthetic applications. Its CAS number 1220521-36-7 serves as a critical identifier for researchers and regulatory compliance.

The compound's isoxazole core is a five-membered aromatic ring containing oxygen and nitrogen, a scaffold widely exploited in drug discovery due to its bioisosteric properties. Recent studies highlight its role in designing kinase inhibitors and antimicrobial agents, aligning with the growing demand for novel therapeutic scaffolds. Researchers frequently search for "3-Bromo-5-(methoxymethyl)isoxazole synthesis" or "CAS 1220521-36-7 suppliers," reflecting its commercial and academic relevance.

In agrochemistry, 3-Bromo-5-(methoxymethyl)isoxazole serves as a precursor for crop protection agents, addressing global concerns about sustainable agriculture. Its methoxymethyl group enhances solubility, a key factor in formulation development. Industry forums often discuss "isoxazole derivatives in pesticide formulation," linking this compound to broader trends in green chemistry.

From a technical perspective, the compound's physical-chemical properties—such as its melting point (typically 80–85°C) and solubility in organic solvents—are critical for process optimization. Analytical methods like HPLC and NMR are routinely employed for quality control, topics frequently queried in scientific databases. The CAS registry 1220521-36-7 ensures traceability in regulatory documentation, a priority for compliance-driven industries.

Emerging applications include its use in material science, particularly in designing photoactive polymers. This aligns with the surge in searches for "functional isoxazoles in OLEDs" and "smart materials," highlighting interdisciplinary potential. Stability studies under varying pH and temperature conditions further expand its utility profiles.

Market analysts note increasing procurement of 1220521-36-7 by contract research organizations (CROs), driven by outsourcing trends in R&D. Keywords like "high-purity 3-Bromo-5-(methoxymethyl)isoxazole" and "custom synthesis CAS 1220521-36-7" reflect niche demands. Storage recommendations (e.g., inert atmosphere, ?20°C) are also frequently searched, underscoring operational considerations.

In summary, 3-Bromo-5-(methoxymethyl)isoxazole (CAS No. 1220521-36-7) exemplifies the convergence of innovation and practicality. Its structural features cater to diverse sectors, from life sciences to advanced materials, while its synthetic accessibility ensures sustained industrial interest. As research evolves, this compound will likely remain pivotal in addressing complex scientific challenges.

• 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)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)