• 1. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?
  Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
• 2. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 3. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
• 4. Excellent electrochemical performance of LiFe0.4Mn0.6PO4 microspheres produced using a double carbon coating process?
  Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
• 5. Enantiomorphic symmetry breaking in crystallization of molten sodium chlorate?
  Martin R. Ward,Gary W. Copeland,Andrew J. Alexander Chem. Commun., 2010,46, 7634-7636

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Nitrobenzenes Nitrophenyl ethers
• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

Comprehensive Overview of 1-(2-Methoxyethoxy)-4-nitrobenzene (CAS No. 22483-40-5): Properties, Applications, and Industry Insights

1-(2-Methoxyethoxy)-4-nitrobenzene (CAS No. 22483-40-5), also known by its systematic name, is a specialized organic compound that has garnered attention in pharmaceutical intermediates, agrochemical synthesis, and material science. This nitro-aromatic derivative features a methoxyethoxy functional group, which enhances its solubility and reactivity in various industrial processes. Researchers and manufacturers frequently search for "1-(2-Methoxyethoxy)-4-nitrobenzene suppliers" or "CAS 22483-40-5 applications," reflecting its niche yet critical role in fine chemical production.

The compound's molecular structure combines a benzene ring substituted with a nitro group (-NO₂) and a 2-methoxyethoxy side chain (-OCH₂CH₂OCH₃). This unique arrangement contributes to its versatility as a building block in organic synthesis. Recent trends in "green chemistry" and "sustainable synthesis" have spurred interest in optimizing its production methods to reduce environmental impact, aligning with global regulatory standards like REACH and FDA guidelines.

In the pharmaceutical sector, 1-(2-Methoxyethoxy)-4-nitrobenzene serves as a precursor for active pharmaceutical ingredients (APIs). Its nitrobenzene core is pivotal in constructing complex molecules, particularly in antiviral and antibacterial drug development. Searches for "nitrobenzene derivatives in medicine" often highlight its relevance. Additionally, its role in dye intermediates and liquid crystal materials makes it valuable in electronics and optoelectronics industries, where "high-purity nitrobenzene compounds" are in demand.

From a technical perspective, the compound exhibits moderate polarity due to its ether and nitro functionalities, making it soluble in common organic solvents like ethanol, acetone, and dimethyl sulfoxide (DMSO). Analytical techniques such as HPLC, GC-MS, and NMR are typically employed for quality control, addressing queries like "CAS 22483-40-5 analysis methods." Storage recommendations emphasize protection from light and moisture to maintain stability, a detail frequently sought by logistics professionals.

Emerging applications in "advanced material science" have further expanded its utility. For instance, researchers explore its incorporation into polymer matrices to modify thermal and optical properties. The compound's compatibility with cross-coupling reactions (e.g., Suzuki-Miyaura) also positions it as a candidate for designing novel organic semiconductors, resonating with searches for "nitro-aromatics in electronics."

Market insights indicate steady growth for 1-(2-Methoxyethoxy)-4-nitrobenzene, driven by Asia-Pacific pharmaceutical and agrochemical industries. Suppliers increasingly emphasize "custom synthesis services" and "scalable production" to meet diverse client needs. Regulatory compliance, particularly concerning workplace safety (e.g., OSHA standards), remains a priority, as evidenced by searches for "safe handling of nitrobenzene derivatives."

In summary, 1-(2-Methoxyethoxy)-4-nitrobenzene (CAS No. 22483-40-5) bridges multiple industries through its synthetic flexibility and functional adaptability. Its alignment with sustainability goals and high-value applications ensures continued relevance in scientific and industrial discourse.

• 100-29-8(1-Ethoxy-4-nitrobenzene)
• 62122-61-6(Ethanol, 2-(3,5-dinitrophenoxy)-)
• 25986-11-2(Benzene,1,1'-[1,2-ethanediylbis(oxy)]bis[3-nitro-)
• 89346-80-5(Benzene, 1-nitro-4-[2-[2-[2-(2-phenoxyethoxy)ethoxy]ethoxy]ethoxy]-)
• 16365-26-7(Ethanol,2-(3-nitrophenoxy)-)
• 62122-63-8(Benzene, 1-(2-methoxyethoxy)-3,5-dinitro-)
• 16365-27-8(2-(p-Nitrophenoxy)ethanol)
• 14467-69-7(1,2-Bis(4-nitrophenoxy)ethane)
• 19157-80-3(Benzenamine,4-[2-(4-nitrophenoxy)ethoxy]-, hydrochloride (1:1))
• 84649-38-7(3,6,9,12,15-Pentaoxaheptadecane, 1,17-bis(4-nitrophenoxy)-)