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2,2'-sulfinylbis(chlorobenzene), also known as 2,2'-dichlorodiphenyl sulfone, is an organic compound with the chemical formula C12H8Cl2O2S. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 95-97°C. 2,2'-sulfinylbis(chlorobenzene) is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is also employed as a chemical intermediate in the production of sulfonamide drugs, which are a class of antibiotics. Due to its reactivity and versatility, 2,2'-sulfinylbis(chlorobenzene) plays a significant role in the chemical industry, contributing to the development of a wide range of products.

5097-08-5

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5097-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5097-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5097-08:
(6*5)+(5*0)+(4*9)+(3*7)+(2*0)+(1*8)=95
95 % 10 = 5
So 5097-08-5 is a valid CAS Registry Number.

5097-08-5Relevant academic research and scientific papers

Synthesis and nano-Pd catalyzed chemoselective oxidation of symmetrical and unsymmetrical sulfides

Li, Xing,Du, Jia,Zhang, Yongli,Chang, Honghong,Gao, Wenchao,Wei, Wenlong

, p. 3048 - 3055 (2019)

A highly chemoselective, efficient and nano-Pd catalyzed protocol for the rapid construction of sulfoxides and sulfones via the oxidation of symmetrical and unsymmetrical sulfides using H2O2 as an oxidant has been developed, respectively. The ready availability of starting materials, easy recovery and reutilization of the catalyst, wide substrate scope, and high yields make this protocol an attractive alternative. The process also involves the metal-free and microwave-promoted synthesis of symmetrical diarylsulfides, and FeCl3-mediated preparation of symmetrical diaryldisulfides through the reaction of arenediazonium tetrafluoroborates with Na2S·9H2O as a sulfur source. In addition, unsymmetrical sulfides were generated via the K2CO3-mediated reaction of arenediazonium tetrafluoroborates with symmetrical disulfides.

Desulfurization of Diaryl(heteroaryl) Sulfoxides with Benzyne

Chen, De-Li,Sun, Yan,Chen, Mengyuan,Li, Xiaojin,Zhang, Lei,Huang, Xin,Bai, Yihui,Luo, Fang,Peng, Bo

supporting information, (2019/06/13)

Two benzyne-enabled desulfurization reactions have been demonstrated which convert diaryl sulfoxides and heteroaryl sulfoxides to biaryls and desulfurized heteroarenes, respectively. The reaction accessing biaryls tolerates a variety of functional groups, such as halides, pseudohalides, and carbonyls. Mechanistic studies reveal that both reactions proceed via a common assembly process but divergent disassemblies of the generated tetraaryl(heteroaryl) sulfuranes.

Palladium-Catalyzed Enantioselective C?H Olefination of Diaryl Sulfoxides through Parallel Kinetic Resolution and Desymmetrization

Zhu, Yu-Chao,Li, Yan,Zhang, Bo-Chao,Zhang, Feng-Xu,Yang, Yi-Nuo,Wang, Xi-Sheng

supporting information, p. 5129 - 5133 (2018/03/27)

The first example of PdII-catalyzed enantioselective C?H olefination with non-chiral or racemic sulfoxides as directing groups was developed. A variety of chiral diaryl sulfoxides were synthesized with high enantioselectivity (up to 99 %) throu

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