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  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
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  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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  Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
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Sulfoximine, S,S-diphenyl-: A Comprehensive Overview

Sulfoximine, also known as S,S-diphenylsulfoximine, is a chemical compound with the CAS registry number 22731-83-5. This compound belongs to the class of organosulfur compounds and has gained significant attention in recent years due to its diverse applications in the pharmaceutical and biotechnology industries.

The structure of S,S-diphenylsulfoximine consists of a sulfoxide core with two phenyl groups attached to the sulfur atom. This unique structure renders it highly reactive and versatile, making it an valuable building block in organic synthesis. Its ability to participate in various chemical reactions, such as nucleophilic substitutions and condensations, has made it a favored intermediate in drug discovery processes.

Recent studies have highlighted the potential of Sulfoximine derivatives in the development of novel therapeutic agents. For instance, research published in the Journal of Medicinal Chemistry (2023) demonstrated that certain sulfoximine-based compounds exhibit potent activity against cancer cells, making them promising candidates for anticancer drug development.

Another area where S,S-diphenylsulfoximine has shown remarkable utility is in the field of biocatalysis. Its ability to act as a chiral auxiliary has been explored extensively, particularly in the synthesis of complex natural products and pharmaceutical intermediates. A study in Biotechnology Journal (2023) reported the successful use of sulfoximine derivatives in asymmetric catalysis, leading to the efficient production of enantiomerically pure compounds.

Moreover, advancements in sulfoximine chemistry have contributed to the development of new materials for bioelectronic drugs. These materials leverage the unique electronic and steric properties of sulfoximine moieties to create novel interfaces between biological systems and electronic devices. This intersection of chemistry and bioelectronics holds immense potential for innovative treatments in neurology and other fields.

Despite its wide-ranging applications, the environmental impact of Sulfoximine and its derivatives remains a critical area of research. Studies are ongoing to evaluate their biodegradability and toxicity, ensuring that these compounds can be used safely in both laboratory settings and commercial applications.

In conclusion, S,S-diphenylsulfoximine stands as a testament to the versatility and innovation of modern organosulfur chemistry. Its role in drug discovery, biocatalysis, and bioelectronics underscores its importance as a key compound in the biomedical sciences. As research continues to uncover new applications and optimize its use, Sulfoximine is poised to play an even more significant role in addressing global health challenges.

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• 33903-50-3((S)-(+)-Methyl Phenyl Sulfoximine)
• 80482-67-3(SULFOXIMINE, N,S-DIMETHYL-S-PHENYL-, (R)-)
• 70975-34-7(SULFOXIMINE, N-BROMO-S,S-DIPHENYL-)
• 22132-97-4(imino(methyl)(4-methylphenyl)-lambda6-sulfanone)
• 635311-89-6((4-fluorophenyl)(imino)methyl-λ?-sulfanone)
• 35543-41-0((4-hydroxyphenyl)(imino)methyl-lambda6-sulfanone)
• 60933-65-5((R)-(-)-S-Methyl-S-phenylsulfoximine)
• 20414-85-1(Sulfoximine,S-methyl-S-(4-methylphenyl)-, [S(R)]-)
• 4381-25-3(imino(methyl)phenyl-λ?-sulfanone)