• 1. An atlas of endohedral Sc2S cluster fullerenes?
  Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
• 2. An apparatus for determining small amounts of alchohol in sour milk and urine
  Analyst, 1964,89, 272-275
• 3. An investigation on the interaction modes of a single-strand DNA aptamer and RBP4 protein: a molecular dynamic simulations approach?
  Raheleh Torabi,Hedayatollah Ghourchian,Massoud Amanlou Org. Biomol. Chem., 2016,14, 8141-8153
• 4. An Assessment of the Laminar Hypersonic Double-Cone Experiments in the LENS-XX Tunnel
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• 5. An amorphous lanthanum–iridium solid solution with an open structure for efficient water splitting?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Styrenes

1-(4-Vinylbenzyl)-1H-imidazole: An Overview of a Versatile Compound (CAS No. 78430-91-8)

1-(4-Vinylbenzyl)-1H-imidazole (CAS No. 78430-91-8) is a versatile organic compound that has garnered significant attention in the fields of organic synthesis, medicinal chemistry, and materials science. This compound is characterized by its unique structural features, which include an imidazole ring and a vinylbenzyl group. These features contribute to its reactivity and potential applications in various scientific and industrial domains.

The imidazole ring is a well-known heterocyclic aromatic compound that plays a crucial role in many biological processes. It is found in several amino acids, such as histidine, and is a key component in many enzymes and receptors. The presence of the imidazole ring in 1-(4-Vinylbenzyl)-1H-imidazole makes it an attractive candidate for the development of new pharmaceuticals and biomaterials.

The vinybenzyl group, on the other hand, provides additional reactivity and functionalization possibilities. This group can undergo various chemical reactions, such as polymerization and cross-linking, making 1-(4-Vinylbenzyl)-1H-imidazole a valuable building block in the synthesis of polymers and copolymers. Recent studies have explored the use of this compound in the development of advanced materials with tailored properties for applications in drug delivery, tissue engineering, and electronic devices.

In the realm of medicinal chemistry, 1-(4-Vinylbenzyl)-1H-imidazole has shown promise as a lead compound for the design of new drugs. Its ability to form stable complexes with metal ions has been exploited in the development of metal-based drugs, which have potential applications in cancer therapy and other diseases. For instance, researchers have synthesized metal complexes of 1-(4-Vinylbenzyl)-1H-imidazole with platinum, copper, and zinc, demonstrating their efficacy as antitumor agents.

Beyond its pharmaceutical applications, 1-(4-Vinylbenzyl)-1H-imidazole has also been investigated for its potential in catalysis. The imidazole ring can act as a ligand for transition metals, forming catalysts that are highly active and selective in various organic transformations. Studies have shown that these catalysts can be used in reactions such as hydrogenation, oxidation, and coupling reactions, offering new avenues for the synthesis of complex molecules.

In materials science, the unique properties of 1-(4-Vinylbenzyl)-1H-imidazole have led to its use in the development of functional polymers and coatings. The vinylbenzyl group allows for easy polymerization with other monomers, resulting in materials with enhanced mechanical strength, thermal stability, and chemical resistance. These properties make the resulting polymers suitable for applications in coatings, adhesives, and composites.

The versatility of 1-(4-Vinylbenzyl)-1H-imidazole extends to its use in sensor technology. The imidazole ring can interact with various analytes through hydrogen bonding or coordination interactions, making it an excellent candidate for the development of chemical sensors. Researchers have developed sensors based on this compound for detecting metal ions, gases, and biomolecules with high sensitivity and selectivity.

In conclusion, 1-(4-Vinylbenzyl)-1H-imidazole (CAS No. 78430-91-8) is a multifaceted compound with a wide range of applications across multiple scientific disciplines. Its unique combination of an imidazole ring and a vinylbenzyl group provides it with exceptional reactivity and functionalization capabilities. Ongoing research continues to uncover new uses for this compound, further solidifying its importance in the fields of organic synthesis, medicinal chemistry, catalysis, materials science, and sensor technology.

• 4238-71-5(1-Benzylimidazole)
• 66335-46-4(Lithium, [1-(phenylmethyl)-1H-imidazol-2-yl]-)
• 56643-83-5(bimb)
• 52461-82-2(1H-Imidazolium, 1-methyl-3-(phenylmethyl)-)
• 78430-93-0(1-[(4-ethenylphenyl)methyl]-2-methyl-1H-Imidazole)
• 78430-92-9(1H-Imidazole, 1-[(3-ethenylphenyl)methyl]-2-methyl-)
• 78430-90-7(1H-Imidazole, 1-[(3-ethenylphenyl)methyl]-)
• 159148-87-5([3-(1H-imidazol-1-ylmethyl)phenyl]methanamine)
• 18994-86-0(1H-Imidazole, 1-[(4-methylphenyl)methyl]-)
• 112086-47-2([4-(imidazol-1-ylmethyl)phenyl]methanamine)