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α-Ethyl-p-methoxybenzyl-phenyl-sulfon, also known as α-ethyl-p-methoxybenzylphenyl sulfone, is an organic compound characterized by a benzyl group attached to a phenyl sulfone moiety. The benzyl group features an ethyl substituent at the α-position and a methoxy group at the para-position relative to the sulfone linkage. α-Ethyl-p-methoxybenzyl-phenyl-sulfon is a white crystalline solid and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its unique structure allows for a range of applications, including the formation of complex molecules and the study of chemical reactivity patterns.

60702-26-3

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60702-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60702-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60702-26:
(7*6)+(6*0)+(5*7)+(4*0)+(3*2)+(2*2)+(1*6)=93
93 % 10 = 3
So 60702-26-3 is a valid CAS Registry Number.

60702-26-3Downstream Products

60702-26-3Relevant academic research and scientific papers

Photocatalyzed site-selective C(sp3)-H sulfonylation of toluene derivatives and cycloalkanes with inorganic sulfinates

Cao, Shi,Gong, Lei,Lin, Yu-Mei,Lu, Cheng,Sha, Liyuan,Zhang, Shaonan

, p. 564 - 570 (2022/02/05)

The development of practical methods for the direct and selective C(sp3)-H functionalization of hydrocarbons is an attractive topic in synthetic chemistry. Although the radical-mediated hydrogen atom transfer (HAT) process has shown considerable potential in such reactions, it still faces fundamental problems associated with reactivity and selectivity. Herein, we report a convenient and economic approach to site-selective C(sp3)-H sulfonylation via photo-induced HAT catalysis. Employing a conjugated polycyclic quinone as a direct HAT photocatalyst, commercially available inorganic sulfinates as the sulfonylation source, copper triflate as an inexpensive oxidant, a variety of toluene derivatives and cycloalkanes were converted into biologically and synthetically interesting sulfone products under mild conditions. The mechanistic studies reveal that the reaction sequence involves direct HAT-induced radical formation and a subsequent copper-mediated organometallic process for the C-S bond formation. This method offers an appealing opportunity to furnish high value-added products from abundant hydrocarbon starting materials and inexpensive reagents.

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