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3,4-dimethoxy-β-methylthio-β-(p-tolylsulfonyl)styrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87228-74-8

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87228-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87228-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87228-74:
(7*8)+(6*7)+(5*2)+(4*2)+(3*8)+(2*7)+(1*4)=158
158 % 10 = 8
So 87228-74-8 is a valid CAS Registry Number.

87228-74-8Relevant academic research and scientific papers

Second-Order Optical Nonlinearities of β-Sulfonylstyrene Derivatives

Sugiyama, Yoshio,Suzuki, Yasushi,Mitamura, Shuichi,Kawamoto, Yugen,Fujita, Makoto,Ogura, Katsuyuki

, p. 3346 - 3348 (1994)

The second-order optical nonlinearities and transparencies of eight substituted styrenes containing at least one sulfonyl group at the β-position, as the electron-withdrawing group, were examined. Oxidation at a sulfur atom (SMe->SOMe->SO2Me) brings about

Reduction of Ketene Dithioacetal S,S-Dioxides with Sodium Borohydride and Its Application to a Convenient Synthesis of Alkyl Arylmethyl Ketones

Ogura, Katsuyuki,Ohtsuki, Kazuo,Takahashi, Kazumasa,Iida, Hirotada

, p. 1597 - 1598 (2007/10/02)

The C-C double bond of a ketene dithioacetal S,S-dioxide was found to undergo reduction with sodium borohydride.This fact provides an efficient synthetic route from an aromatic aldehyde to an alkyl arylmethyl ketone using methylthiomethyl p-totyl sulfone.

UTILIZATION OF METHYLTHIOMETHYL p-TOLYL SULFONE IN ORGANIC SYNTHESIS

Ogura, Katsuyuki,Yahata, Nobuhiro,Hashizume, Kimitoshi,Tsuyama, Koichi,Takahashi, Kazumasa,Iida, Hirotada

, p. 767 - 770 (2007/10/02)

Methylthiomethyl p-tolyl sulfone was found to be one of the useful reagents for preparation of various organic compounds such as S-methyl α-ketocarbothioates, carboxylic esters, five- and six-membered cycloalkanones, and α-methoxy-α-arylacetic esters.

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