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4,6-dimethoxy-5,5-dimethyl-7-(p-tolylthio)hept-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

359701-09-0

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359701-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359701-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,7,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 359701-09:
(8*3)+(7*5)+(6*9)+(5*7)+(4*0)+(3*1)+(2*0)+(1*9)=160
160 % 10 = 0
So 359701-09-0 is a valid CAS Registry Number.

359701-09-0Downstream Products

359701-09-0Relevant academic research and scientific papers

Structure and reactivity of thiophanium salts, the elusive intermediates in ArS+-mediated one-pot sequence of three Ad(E) reactions

Lazareva, Margarita I.,Kryschenko, Yury K.,Caple, Ron,Wakefield, Darren,Hayford, Anthony,Smit, William A.,Shashkov, Alexander S.

, p. 8787 - 8790 (1998)

The structure of the previously postulated cationoid intermediate, presumably formed in ArS+-mediated coupling of two vinyl ether units, was firmly established as (1R*,2R*,4S*)-2,4-dimethoxy-3,3-dimethyl-1-p- tolylthiophanium salt and its reactivity was elucidated.

Polyfunctional compounds containing the 4,6-dialkoxy-7-arylthioheptene moiety as synthetically useful intermediates. The course of Lewis acid-induced transformations

Chekmarev, Dmitriy S.,Lazareva, Margarita I.,Zatonsky, Georgy V.,Maskaev, Andrei V.,Caple, Ron,Smit, William

, p. 7957 - 7967 (2007/10/03)

Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products containing either cyclohexane or 1,3-diene units are described.

Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety

Chekmarev,Maskaev,Zatonsky,Lazareva,Caple,Smit

, p. 176 - 178 (2007/10/03)

The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.

Four-component coupling via a sequence of three AdE reactions involving arenesulfenyl chloride, two alkyl vinyl ether units, and silicon-containing π-donors as a method for the synthesis of polyfunctional compounds

Lazareva,Kryschenko,Dilman,Hayford,Caple,Smit

, p. 895 - 903 (2007/10/03)

A protocol for the synthesis of polyfunctional compounds by a Lewis acid initiated tandem sequence of three AdE reactions of sulfur-containing electrophiles with two alkyl vinyl ether units and silicon containing π-donors is proposed.

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