• 1. Distinct roles of SNARE-mimicking lipopeptides during initial steps of membrane fusion?
  Alena Koukalová,?árka Pokorná,Aimee L. Boyle,Nestor Lopez Mora,Alexander Kros,Martin Hof,Radek ?achl Nanoscale, 2018,10, 19064-19073
• 2. Fe3O4 nanoparticle chains with N-doped carbon coating: magnetotactic bacteria assisted synthesis and high-rate lithium storage?
  Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
• 3. Evidence of rutile-to-anatase photo-induced electron transfer in mixed-phase TiO2 by solid-state NMR spectroscopy?
  Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
• 4. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 5. Evolution and characterization of a benzylguanine-binding RNA aptamer?
  J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic phosphonic acids and derivatives Phosphonic acid diesters Dialkyl alkylphosphonates

Comprehensive Guide to Diethyl (ethoxymethyl)phosphonate (CAS No. 10419-80-4): Properties, Applications, and Innovations

Diethyl (ethoxymethyl)phosphonate (CAS No. 10419-80-4) is a specialized organophosphorus compound with a wide range of applications in organic synthesis, pharmaceuticals, and material science. Known for its unique phosphonate ester structure, this chemical has garnered significant attention due to its versatility as a building block in modern chemistry. Researchers and industries value its role in facilitating C-P bond formation, a critical step in synthesizing bioactive molecules and advanced materials.

The compound's molecular formula, C₇H₁₇O₄P, highlights its ethoxy and phosphonate functional groups, which contribute to its reactivity and solubility in organic solvents. Its CAS number 10419-80-4 is frequently searched in chemical databases, reflecting its importance in academic and industrial research. Recent trends show growing interest in sustainable synthesis methods, aligning with global demands for greener chemistry. Diethyl (ethoxymethyl)phosphonate is often discussed in the context of atom-efficient reactions and catalytic processes, making it a hotspot for innovation.

One of the most searched questions about this compound revolves around its synthetic applications. For instance, it serves as a key intermediate in the preparation of α-aminophosphonates, which are pivotal in drug discovery for their bioactivity. Another trending topic is its use in flame retardants and coating additives, where its phosphorus content enhances material properties. These applications are frequently explored in patents and scientific literature, driving further interest in CAS 10419-80-4.

From a technical perspective, Diethyl (ethoxymethyl)phosphonate exhibits stability under standard conditions but requires careful handling due to its sensitivity to moisture. Its boiling point and refractive index are often cited in purity assessments, ensuring quality control in industrial batches. Analytical techniques like NMR spectroscopy and GC-MS are commonly employed to characterize this compound, addressing another frequent query among researchers.

In the context of green chemistry, recent studies focus on optimizing the synthesis of Diethyl (ethoxymethyl)phosphonate to reduce waste and energy consumption. This aligns with broader industry shifts toward circular economy principles. Additionally, its potential in agrochemical formulations has sparked discussions about eco-friendly pest control solutions, a trending topic in sustainable agriculture.

As the demand for high-performance chemicals grows, Diethyl (ethoxymethyl)phosphonate continues to be a subject of cutting-edge research. Its compatibility with microwave-assisted synthesis and flow chemistry techniques positions it as a forward-looking candidate for scalable production. For those searching "CAS 10419-80-4 suppliers" or "phosphonate derivatives uses," this compound represents a bridge between traditional chemistry and modern technological advancements.

• 64226-00-2(Phosphonic acid, [(2-propenyloxy)methyl]-, diethyl ester)
• 116384-57-7(1-bromo-2-(diethoxyphosphorylmethoxy)ethane)
• 32806-04-5(Diethyl (Methoxymethyl)phosphonate)
• 160713-49-5(diethyl [(2-aminoethoxy)methyl]phosphonate)
• 3084-40-0(Diethyl P-(Hydroxymethyl)phosphonic Acid Ester)
• 139578-84-0(Phosphonic acid, [(ethenyloxy)methyl]-, diethyl ester)
• 116384-56-6(Diethyl ((2-chloroethoxy)methyl)phosphonate)
• 59463-48-8
• 116384-55-5(Diethyl 2-hydroxyethoxymethanephosphonate)
• 162612-60-4(Phosphonic acid, [(2-hydroxyethoxy)methyl]-, bis(1-methylethyl) ester)