• 1. Emulsion technologies for multicellular tumour spheroid radiation assays?
  Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
• 2. Excitation energies from ground-state density-functionals by means of generator coordinates
  A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
• 3. Evidence for the intrinsic nature of band-gap states electrochemically observed on atomically flat TiO2(110) surfaces?
  Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
• 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. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzotriazoles

Comprehensive Overview of Ethyl 1-isopropyl-1,2,3-benzotriazole-5-carboxylate (CAS No. 1352217-61-8)

Ethyl 1-isopropyl-1,2,3-benzotriazole-5-carboxylate (CAS No. 1352217-61-8) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and material science. This benzotriazole derivative is characterized by its unique molecular structure, which combines an ethyl carboxylate group with an isopropyl-substituted benzotriazole core. The compound's versatility makes it a valuable intermediate in synthetic chemistry, particularly in the development of novel bioactive molecules.

In recent years, the demand for benzotriazole-based compounds has surged due to their wide-ranging applications. Researchers and industry professionals frequently search for terms like "benzotriazole derivatives," "ethyl carboxylate synthesis," and "CAS 1352217-61-8 applications" to explore its potential. The compound's stability and reactivity profile make it an ideal candidate for drug discovery and agrochemical formulation, aligning with the growing interest in sustainable and efficient chemical solutions.

One of the most compelling aspects of Ethyl 1-isopropyl-1,2,3-benzotriazole-5-carboxylate is its role in heterocyclic chemistry. Heterocycles are a cornerstone of modern medicinal chemistry, and this compound's benzotriazole scaffold offers a robust platform for further functionalization. Its ethyl carboxylate moiety enhances solubility and bioavailability, making it a preferred choice for researchers working on bioactive molecules. This aligns with the current trend of optimizing ADME properties (Absorption, Distribution, Metabolism, and Excretion) in pharmaceutical development.

The synthesis of Ethyl 1-isopropyl-1,2,3-benzotriazole-5-carboxylate involves multi-step organic reactions, often starting from readily available benzotriazole precursors. Advanced techniques such as microwave-assisted synthesis and catalytic hydrogenation have been employed to improve yield and purity. These methods resonate with the industry's shift toward green chemistry and process optimization, which are frequently searched topics in academic and industrial circles.

Beyond pharmaceuticals, this compound has found utility in material science, particularly in the development of corrosion inhibitors and UV stabilizers. The benzotriazole ring system is known for its ability to absorb ultraviolet radiation, making it a key component in coatings and polymers. This application is highly relevant to industries focused on durable materials and environmental sustainability, addressing the global demand for longer-lasting and eco-friendly products.

In conclusion, Ethyl 1-isopropyl-1,2,3-benzotriazole-5-carboxylate (CAS No. 1352217-61-8) stands out as a multifaceted compound with broad applications. Its significance in drug discovery, agrochemicals, and material science underscores its importance in contemporary research. As the scientific community continues to explore its potential, this compound is poised to play a pivotal role in advancing innovation across multiple disciplines.

• 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)