• 1. Aluminium alkyl and aryloxide complexes of pyrazine and bipyridines: synthesis and structure?
  Doug Ogrin,Laura H. van Poppel,Simon G. Bott,Andrew R. Barron Dalton Trans., 2004, 3689-3694
• 2. Acenaphthenic hopanoids, a novel series of aromatised
  Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
• 3. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
  Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
• 4. An artificial enzyme cascade amplification strategy for highly sensitive and specific detection of breast cancer-derived exosomes?
  Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
• 5. An approach to 7-aza-1-phosphanorbornane complexes: strain promoted rearrangement of 1-iminylphosphirane complexes and cycloaddition with olefins?
  Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526

• Solvents and Organic Chemicals Organic Compounds Benzenoids Tetralins Tetralins
• Solvents and Organic Chemicals Organic Compounds Benzenoids Tetralins

a-Tetralone-13C6: A Comprehensive Overview

a-Tetralone-13C6 (CAS No. 189811-58-3) is a highly specialized compound that has garnered significant attention in the fields of organic chemistry, pharmaceutical research, and materials science. This compound is a derivative of tetralone, a bicyclic aromatic ketone, with six carbon atoms enriched with the 13C isotope. The incorporation of 13C6 into the molecular structure makes it an invaluable tool for advanced spectroscopic studies, particularly in nuclear magnetic resonance (NMR) spectroscopy, where it serves as a stable isotope-labeled reference compound.

The synthesis of a-Tetralone-13C6 involves a multi-step process that combines traditional organic synthesis techniques with isotopic enrichment methods. Recent advancements in catalytic asymmetric synthesis have enabled the production of this compound with high purity and isotopic fidelity. Researchers have explored various catalyst systems, including palladium-catalyzed cross-couplings and enantioselective reductions, to optimize the synthesis pathway. These developments have not only improved the yield but also reduced the environmental footprint of the manufacturing process.

In terms of applications, a-Tetralone-13C6 has found extensive use in the pharmaceutical industry as a building block for complex molecules. Its rigid bicyclic structure provides a versatile scaffold for drug design, particularly in the development of kinase inhibitors and other bioactive compounds. For instance, recent studies have demonstrated its utility in constructing heterocyclic frameworks that exhibit potent anti-cancer activity. Additionally, its isotopic labeling makes it an ideal candidate for metabolic studies, where it can be used to track molecular transformations in vivo.

The chemical properties of a-Tetralone-13C6 are well-documented, with a melting point of approximately 250°C and a boiling point exceeding 400°C under standard conditions. Its solubility profile shows moderate solubility in common organic solvents such as dichloromethane and acetonitrile, making it suitable for various analytical techniques. The compound's stability under thermal and oxidative conditions has been thoroughly investigated, with recent studies highlighting its resistance to degradation under mild reaction conditions.

From an environmental perspective, a-Tetralone-13C6 exhibits low toxicity and minimal bioaccumulation potential, which aligns with current regulatory standards for chemical safety. Its production and handling processes are designed to minimize waste generation and ensure compliance with green chemistry principles. This commitment to sustainability has positioned a-Tetralone-13C6 as a preferred choice in eco-friendly chemical manufacturing.

Looking ahead, the demand for a-Tetralone-13C6 is expected to grow significantly as researchers continue to uncover its potential in emerging fields such as optoelectronics and nanotechnology. Its unique electronic properties make it a promising candidate for applications in organic light-emitting diodes (OLEDs) and flexible electronics. Furthermore, advancements in computational chemistry are enabling researchers to predict its reactivity more accurately, paving the way for novel synthetic routes and functionalized derivatives.

In conclusion, a-Tetralone-13C6 (CAS No. 189811-58-3) stands out as a versatile and valuable compound with diverse applications across multiple disciplines. Its isotopic labeling feature not only enhances its utility in analytical chemistry but also underscores its importance in cutting-edge research initiatives. As scientific understanding deepens and technological innovations continue to unfold, a-Tetralone-13C6 is poised to play an even more pivotal role in shaping the future of chemical sciences.

• 83-33-0(2,3-dihydro-1H-inden-1-one)
• 24623-20-9(6-Methyl-1-indanone)
• 4600-82-2(5-Ethyl-2,3-dihydro-1H-inden-1-one)
• 4593-38-8(5-Methyl-1-indanone)
• 24644-78-8(4-Methyl-2,3-dihydro-1H-inden-1-one)
• 826-73-3(6,7,8,9-tetrahydro-5H-benzo7annulen-5-one)
• 1590-08-5(2-methyl-1,2,3,4-tetrahydronaphthalen-1-one)
• 2040-14-4(2'-Methylpropiophenone)
• 19832-98-5(4-methyl-1,2,3,4-tetrahydronaphthalen-1-one)
• 529-34-0(1,2,3,4-tetrahydronaphthalen-1-one)