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1-[(4-fluoro-phenylsulfanyl)-methyl]-4-methoxy-benzene is a complex organic compound with the molecular formula C14H13FO2S. It features a benzene ring with a methoxy group at the 4-position, a 4-fluorophenylsulfanyl group attached to a methyl group at the 1-position, and a sulfur atom connecting the two aromatic rings. 1-[(4-fluoro-phenylsulfanyl)-methyl]-4-methoxy-benzene is characterized by its unique structure, which includes fluorine and sulfur atoms, making it potentially useful in various chemical and pharmaceutical applications. Its properties, such as reactivity and solubility, can be influenced by the presence of these heteroatoms, and it may be of interest in the synthesis of more complex molecules or as a precursor in organic chemistry.

1426-52-4

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1426-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1426-52:
(6*1)+(5*4)+(4*2)+(3*6)+(2*5)+(1*2)=64
64 % 10 = 4
So 1426-52-4 is a valid CAS Registry Number.

1426-52-4Relevant academic research and scientific papers

Dechalcogenization of Aryl Dichalcogenides to Synthesize Aryl Chalcogenides via Copper Catalysis

Cao, Fei,Chen, Jinhong,Deng, Jiedan,Deng, Xuemei,Hou, Yongsheng,Shao, Xiangfeng,Shi, Tao,Wang, Yongqiang,Wang, Zhen,Wu, Lingxi,Yang, Jinru,Yang, Yuhang

, p. 2707 - 2712 (2020)

An application for dechalcogenization of aryl dichalcogenides via copper catalysis to synthesize aryl chalcogenides is disclosed. This approach is highlighted by the practical conditions, broad substrate scope, and good functional group tolerance with several sensitive groups such as aldehyde, ketone, ester, amide, cyanide, alkene, nitro, and methylsulfonyl. Furthermore, the robustness of this methodology is depicted by the late-stage modification of estrone and synthesis of vortioxetine. Remarkably, synthesis of more challenging organic materials with large ring tension under milder conditions and synthesis of some halogen contained diaryl sulfides which could not be synthesized using metal-catalyzed coupling reactions of aryl halogen are successfully accomplished with this protocol.

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