• 1. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 2. Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components?
  Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
• 3. Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond?
  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
• 4. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 5. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridine carboxaldehydes

Introduction to 6-Ethylpyridine-2-Carbaldehyde (CAS No. 153646-82-3)

The compound 6-Ethylpyridine-2-Carbaldehyde, identified by the CAS registry number CAS No. 153646-82-3, is a significant organic chemical entity with a diverse range of applications in various scientific and industrial fields. This compound belongs to the class of pyridine derivatives, which are widely studied due to their unique chemical properties and potential for use in pharmaceuticals, agrochemicals, and materials science.

The molecular structure of 6-Ethylpyridine-2-Carbaldehyde consists of a pyridine ring substituted with an ethyl group at the sixth position and an aldehyde group at the second position. This substitution pattern imparts specific electronic and steric properties to the molecule, making it a versatile building block in organic synthesis. The compound's structure allows for various functional group transformations, enabling its use in the construction of more complex molecules with desired biological or chemical activities.

Recent studies have highlighted the potential of pyridine derivatives like 6-Ethylpyridine-2-Carbaldehyde in drug discovery. Researchers have explored its role as a precursor for bioactive compounds, particularly in the development of anti-inflammatory and anticancer agents. For instance, a study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit promising inhibitory activity against certain enzymes associated with inflammatory pathways.

In addition to its pharmacological applications, 6-Ethylpyridine-2-Carbaldehyde has also found utility in materials science. Its ability to form stable coordination complexes with transition metals has led to its investigation as a ligand in catalytic processes. Recent advancements in asymmetric catalysis have utilized this compound to enhance the selectivity and efficiency of reactions, making it a valuable tool in green chemistry.

The synthesis of 6-Ethylpyridine-2-Carbaldehyde typically involves multi-step organic reactions, often starting from simpler pyridine precursors. One common approach is the alkylation of pyridine followed by oxidation to introduce the aldehyde group. This process has been optimized in recent years through the use of environmentally friendly reagents and conditions, aligning with current trends toward sustainable chemical practices.

In terms of physical properties, 6-Ethylpyridine-2-Carbaldehyde is known for its moderate solubility in organic solvents and its relatively high melting point, which makes it suitable for solid-state reactions and crystallization studies. Its thermal stability has also been a focus of recent research, with studies indicating that it can withstand certain reaction conditions without significant degradation.

The application of computational chemistry techniques has further enhanced our understanding of this compound's properties. Quantum mechanical calculations have provided insights into its electronic structure and reactivity, aiding in the design of more efficient synthetic routes and predictive modeling for potential applications.

In conclusion, 6-Ethylpyridine-2-Carbaldehyde (CAS No. 153646-82-3) stands as a testament to the ongoing advancements in organic chemistry and materials science. Its versatility as a chemical building block, combined with its promising bioactivity profiles, positions it as a key compound for future research and industrial applications.

• 31685-34-4(1,1'-(1H-pyrrole-2,5-diyl)bis-Ethanone)
• 102878-26-2(ketone,6-ethyl-2-pyridylmethyl)
• 6982-72-5(1-(5-methyl-1H-pyrrol-2-yl)-Ethanone)
• 6940-57-4(1-(6-methyl-2-pyridyl)ethanone)
• 1122-62-9(1-(pyridin-2-yl)ethan-1-one)
• 1129-30-2(2,6-Diacetylpyridine)
• 20857-21-0(2-Pyridinecarboxaldehyde,6-acetyl-)
• 153646-83-4(6-(1-methylethyl)-2-Pyridinecarboxaldehyde)
• 208111-24-4(2-Pyridinecarboxaldehyde, 6-cyclopropyl- (9CI))
• 30440-88-1(Ethanone,1-(pyridinyl)-)