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(E)-(1-(4-bromophenyl)-2-tosylprop-1-en-1-yl)(phenyl)selane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82721-75-3

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82721-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82721-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82721-75:
(7*8)+(6*2)+(5*7)+(4*2)+(3*1)+(2*7)+(1*5)=133
133 % 10 = 3
So 82721-75-3 is a valid CAS Registry Number.

82721-75-3Relevant academic research and scientific papers

Copper-Catalyzed Three Component Regio- and Stereospecific Selenosulfonation of Alkynes: Synthesis of (E)-β-Selenovinyl Sulfones

Liu, Yang,Zheng, Guangfan,Zhang, Qian,Li, Yan

, p. 2269 - 2275 (2017)

A copper-catalyzed highly regio- and stereospecific selenosulfonation of alkynes with arylsulfonohydrazides and diphenyl diselenide has been developed. This novel three component reaction proceeds under very mild conditions and with a broad scope of substrates, providing a wide range of (E)-β-selenovinyl sulfones in good to excellent yields.

Synthesis of (E)-β-Selenovinyl Sulfones through a Multicomponent Regio- and Stereospecific Selenosulfonation of Alkynes with Insertion of Sulfur Dioxide

Sun, Kai,Shi, Zuodong,Liu, Zhenhua,Luan, Baixue,Zhu, Jiali,Xue, Yanru

supporting information, p. 6687 - 6690 (2018/11/21)

A novel and practical method for the selenosulfonation of alkynes with the insertion of sulfur dioxide has been developed. A series of β-(seleno)vinyl sulfones with high levels of regio- and stereoselectivity have been prepared. The key features of this reaction include a broad substrate scope, excellent functional-group tolerance, and amenability to scale-up synthesis. A plausible radical mechanism is proposed to illustrate this reaction.

Solid-phase synthesis of β-keto sulfones

Qian, Hao,Huang, Xian

, p. 1934 - 1936 (2007/10/03)

A novel method for the preparation of β-keto-sulfones through the use of organoselenium reagents in the solid phase by polystyrene-supported benzeneselenosulfonate or tolueneseleno-sulfonate with acetylenes has been developed. Georg Thieme Verlag Stuttgart.

Addition of Phenyl Areneselenosulphonates to Acetylenes: a Route to Acetylenic Sulphones

Miura, Takashi,Kobayashi, Michio

, p. 438 - 439 (2007/10/02)

Treatment of phenyl areneselenosulphonates (1) with terminal acetylenes resulted in the formation of β-(phenylseleno)vinyl sulphones (2), which on treatment with excess of hydrogen peroxide in tetrahydrofuran at room temperature gave acetylenic sulphones

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