• 1. Synthesis, kinetics, and characterization of bio-based thermosets obtained through polymerization of a 2,5-furandicarboxylic acid-based bis(2-oxazoline) with sebacic acid
  Carolus H. R. M. Wilsens,Nino J. M. Wullems,Erik Gubbels,Yefen Yao,Sanjay Rastogi,Bart A. J. Noordover Polym. Chem. 2015 6 2707
• 2. Intrinsic low dielectric behaviour of a highly thermally stable Sr-based metal–organic framework for interlayer dielectric materials
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• 3. Influence of mechanical, thermal, and electrical perturbations on the dielectric behaviour of guest-encapsulated HKUST-1 crystals
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzene and substituted derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives
• Solvents and Organic Chemicals Organic Compounds Heterocyclic Compounds

Comprehensive Overview of 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene (CAS No. 34052-90-9)

1,3-Bis(4,5-dihydrooxazol-2-yl)benzene, identified by its CAS number 34052-90-9, is a specialized organic compound widely recognized for its unique structural properties and applications in advanced material science. This compound belongs to the class of bis-oxazoline derivatives, which are increasingly gaining attention due to their versatility in catalysis, polymer modification, and pharmaceutical intermediates. The presence of two oxazoline rings attached to a benzene core enhances its reactivity and binding capabilities, making it a valuable building block in synthetic chemistry.

In recent years, the demand for high-performance ligands and chiral auxiliaries has surged, driven by advancements in asymmetric synthesis and green chemistry. Researchers and industries are actively exploring compounds like 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene for their ability to facilitate stereoselective reactions, a topic frequently searched in academic and industrial forums. Its role in metal-organic frameworks (MOFs) and coordination polymers has also been a focal point, aligning with the growing interest in sustainable materials and nanotechnology.

The compound's thermal stability and solubility profile make it suitable for diverse solvent systems, a feature often queried in chemical databases. Users frequently search for "solubility of bis-oxazoline derivatives" or "applications of CAS 34052-90-9," reflecting its relevance in both laboratory and industrial settings. Additionally, its potential in photoactive materials and catalysis has been highlighted in recent publications, addressing the need for eco-friendly alternatives in chemical manufacturing.

From a synthetic perspective, 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene is often synthesized via cyclization reactions involving benzonitrile derivatives and amino alcohols. This process is a common subject in organic chemistry tutorials, with searches like "synthesis of bis-oxazoline ligands" trending among students and professionals. The compound's electron-rich nature further enables its use in cross-coupling reactions, a technique pivotal in drug discovery and material science.

In the context of polymer science, this compound serves as a chain extender or cross-linking agent, contributing to the mechanical strength and durability of engineered plastics. Queries such as "bis-oxazoline in polymer modification" underscore its industrial significance. Moreover, its compatibility with biodegradable polymers aligns with the global push toward sustainable packaging solutions, a hot topic in environmental science.

Safety and handling of CAS 34052-90-9 are also frequently discussed, with users seeking information on storage conditions and compatibility with other reagents. While not classified as hazardous, proper handling protocols are emphasized in technical datasheets, catering to the laboratory safety awareness trend. The compound's stability under ambient conditions is another advantage, reducing logistical challenges in procurement and storage.

In summary, 1,3-Bis(4,5-dihydrooxazol-2-yl)benzene (CAS No. 34052-90-9) is a multifaceted compound bridging gaps between academia and industry. Its applications in asymmetric synthesis, material science, and green chemistry resonate with current research priorities, making it a subject of continuous exploration and innovation.

• 40054-08-8(2-naphthalen-1-yl-4,5-dihydro-1,3-oxazole)
• 54472-44-5(Oxazole, 2,2'-(1,2-phenylene)bis[4,5-dihydro-)
• 649536-59-4(Oxazole, 2,2'-(1,8-anthracenediyl)bis[4,5-dihydro-)
• 7127-19-7(2-Phenyl-4,5-dihydrooxazole)
• 54472-46-7(Benzenamine, 4-(4,5-dihydro-2-oxazolyl)-)
• 649536-54-9(Oxazole, 2,2'-(1,5-naphthalenediyl)bis[4,5-dihydro-)
• 686753-00-4(Oxazole, 2-(3,5-dimethylphenyl)-4,5-dihydro-)
• 61260-45-5(Oxazole, 4,5-dihydro-4-methyl-2-phenyl-, (S)-)
• 75953-88-7(Oxazole, 2,2',2''-(1,3,5-benzenetriyl)tris[4,5-dihydro-)
• 7426-75-7(1,4-Bis(4,5-dihydro-2-oxazolyl)benzene)