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1-Phenyl-2-phenylmethanesulfinylethanone is an organic compound with the molecular formula C16H14OS. It is a derivative of ethanone, featuring a phenyl group attached to the first carbon and a phenylmethanesulfinyl group attached to the second carbon. The phenylmethanesulfinyl group consists of a phenyl ring connected to a methanesulfinyl moiety, which is a sulfur-containing functional group. 1-phenyl-2-phenylmethanesulfinylethanone is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its complex structure, it is often synthesized through multi-step reactions and may exhibit interesting reactivity patterns, making it a subject of interest for chemists studying the behavior of sulfur-containing organic compounds.

6099-26-9

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6099-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6099-26-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6099-26:
(6*6)+(5*0)+(4*9)+(3*9)+(2*2)+(1*6)=109
109 % 10 = 9
So 6099-26-9 is a valid CAS Registry Number.

6099-26-9Relevant academic research and scientific papers

A route to benzylic arylsulfoxides from β-ketosulfoxides

Chang, Meng-Yang,Cheng, Yu-Chieh,Chan, Chieh-Kai

, p. 4068 - 4075 (2016/07/06)

The K2CO3-mediated benzylation of β-ketosulfoxides 4 with 2.0?equiv of benzylic halides 5 affords benzylic arylsulfoxides 6 in moderate yields along with trace amounts of chalcones 7. The products 6 are assumed to form in situ intermediates of sulfenate anions from β-ketosulfoxides which are commonly involved in carbon–sulfur bond formation. A plausible mechanism has been proposed.

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