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1-(phenylsulfinyl)-4-(phenylsulfinyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59090-58-3

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59090-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59090-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59090-58:
(7*5)+(6*9)+(5*0)+(4*9)+(3*0)+(2*5)+(1*8)=143
143 % 10 = 3
So 59090-58-3 is a valid CAS Registry Number.

59090-58-3Downstream Products

59090-58-3Relevant academic research and scientific papers

Palladium/PC-Phos-Catalyzed Enantioselective Arylation of General Sulfenate Anions: Scope and Synthetic Applications

Wang, Lei,Chen, Mingjie,Zhang, Peichao,Li, Wenbo,Zhang, Junliang

, p. 3467 - 3473 (2018/03/13)

Herein we reported an efficient palladium-catalyzed enantioselective arylation of both alkyl and aryl sulfenate anions to deliver various chiral sulfoxides in good yields (up to 98%) with excellent enantioselectivities (up to 99% ee) by the use of our developed chiral O,P-ligands (PC-Phos). PC-Phos are easily prepared in short steps from inexpensive commercially available starting materials. The single-crystal structure of the PC4/PdCl2 showed that a rarely observed 11-membered ring was formed via the O,P-coordination with the palladium(II) center. The salient features of this method include general substrate scope, ease of scale-up, applicable to the late-stage modification of bioactive compounds, and the synthesis of a marketed medicine Sulindac.

Selective aerobic oxidation of sulfides to sulfoxides catalyzed by coenzyme NAD+ models

Xu, Hua-Jian,Lin, Yi-Cheng,Wan, Xin,Yang, Chun-Yan,Feng, Yi-Si

experimental part, p. 8823 - 8827 (2011/01/04)

Coenzyme NAD+ models can be applied in the photooxygenation of sulfides to sulfoxides as organocatalysts at room temperature. A series of sulfoxides are synthesized easily with this protocol and the possible mechanism is discussed. This procedure provides a reliable approach to the clean production of useful sulfoxides in synthetic chemistry.

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