• 1. 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
• 2. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 3. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
• 4. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 5. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847

2-Amino-5-Ethylphenol: A Comprehensive Overview

2-Amino-5-Ethylphenol, also known by its CAS number 182499-90-7, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound, characterized by its unique structure featuring an amino group and an ethyl substituent on a phenol ring, has garnered attention due to its potential in drug design, polymer synthesis, and as an intermediate in chemical manufacturing. Recent advancements in synthetic methodologies and its biological evaluations have further highlighted its importance in contemporary research.

The molecular structure of 2-Amino-5-Ethylphenol consists of a benzene ring with hydroxyl (-OH) and amino (-NH2) groups at the 2nd and 5th positions, respectively, along with an ethyl group attached at the 5th position. This arrangement imparts the compound with unique electronic properties, making it a valuable substrate for various chemical transformations. The presence of both amino and hydroxyl groups allows for multiple reaction pathways, including nucleophilic substitutions, condensations, and oxidations, which are exploited in diverse synthetic strategies.

Recent studies have focused on the synthesis of 2-Amino-5-Ethylphenol via novel routes that enhance yield and selectivity. For instance, researchers have employed catalytic hydrogenation techniques to streamline the production process, reducing both time and cost. Additionally, green chemistry approaches have been integrated into its synthesis, utilizing renewable feedstocks and minimizing environmental impact. These advancements underscore the compound's relevance in sustainable chemical manufacturing.

In the pharmaceutical industry, 2-Amino-5-Ethylphenol has shown promise as a lead compound for drug development. Its ability to act as a bioisostere or pharmacophore mimic makes it a valuable tool in medicinal chemistry. Recent research has explored its potential as an anti-inflammatory agent, leveraging its ability to modulate key enzymes involved in inflammatory pathways. Furthermore, studies into its antioxidant properties suggest applications in neuroprotective therapies, where oxidative stress plays a pivotal role.

The material science sector has also benefited from the properties of 2-Amino-5-Ethylphenol. Its use as a precursor in polymer synthesis has led to the development of novel materials with enhanced mechanical and thermal stability. Researchers have successfully incorporated this compound into polyurethane formulations, resulting in materials with improved durability under harsh conditions. Such innovations highlight its role as a key building block in advanced material engineering.

Beyond these applications, 2-Amino-5-Ethylphenol has emerged as an important intermediate in the synthesis of more complex organic molecules. Its ability to undergo multiple functional group transformations makes it indispensable in multi-step synthesis protocols. Recent advancements have seen its use in the construction of heterocyclic compounds, which are critical components in modern drug discovery.

In conclusion, 2-Amino-5-Ethylphenol (CAS No: 182499-90-7) stands as a testament to the versatility of organic compounds in modern science. With ongoing research uncovering new synthetic pathways and expanding its application domains, this compound continues to be a focal point for innovation across multiple disciplines. Its role as both a functional material and a pharmacological agent ensures that it remains at the forefront of chemical research for years to come.

• 22428-30-4(5,5'-Methylenebis(2-aminophenol))
• 3280-68-0(2-Amino-4-isopropylphenol)
• 104083-77-4(Phenol,2-amino-5-(2-aminoethyl)-)
• 149861-22-3(2-Amino-5-ethylphenol hydrochloride)
• 887141-18-6(Phenol,2-amino-5-propyl-)
• 16523-28-7(2-Amino-4-(3-amino-4-hydroxybenzyl)phenol)
• 436088-33-4(Phenol,2-amino-5-(1-methylpropyl)-)
• 94109-11-2(2-Amino-4-ethylphenol)
• 6423-19-4(Phenol,4,4'-methylenebis[3-amino-)
• 2835-98-5(2-Amino-5-methylphenol)