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1-(p-methylbenzenesulfonyl)-1,3-butadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85615-58-3

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85615-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85615-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,1 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85615-58:
(7*8)+(6*5)+(5*6)+(4*1)+(3*5)+(2*5)+(1*8)=153
153 % 10 = 3
So 85615-58-3 is a valid CAS Registry Number.

85615-58-3Relevant academic research and scientific papers

"Syn effect" in nucleophilic addition of amines to 1,3-dienyl sulfone and ethyl (E)-2,4-pentadienoate

Yamazaki, Masao,Guha, Samar Kumar,Ukaji, Yutaka,Inomata, Katsuhiko

experimental part, p. 740 - 753 (2009/04/10)

The stereochemistry of nucleophilic addition of amines to (E)-l-tosyl-l,3-butadiene was investigated. The Z/E ratios of the resulting allylic sulfones varied with amines, solvents, temperature, and concentration. When diethylamine was reacted in low conce

Diazo reactions with unsaturated compounds: XI. Reactions of benzene-, p-methylbenzene-, and p-methoxybenzenesulfonyl-1,3-butadienes with arenediazonium chlorides and 1-aryl-3,3-dimethyl-1-triazenes

Smalius,Naidan

, p. 1295 - 1298 (2008/02/04)

1-(p-Methylbenzene)-and 1-(p-methoxybenzenesulfonyl)-1,3-butadienes in aqueous acetone in the presence of copper(I) or copper(II) chlorides react with arenediazonium chlorides and 1-aryl-3,3-dimethyl-1-triazenes to form 1-(p-methylbenzene)-and 1-(p-methox

Synthesis of Allyl and Dienyl Sulphones via Iodosulphonylation of Conjugated Dienes

Barluenga, Jose,Martinez-Gallo, Jose M.,Najera, Carmen,Fananas, Francisco J.,Yus, Miguel

, p. 2605 - 2610 (2007/10/02)

The iodosulphonylation of conjugated dienes with sodium or mercury(II) toluene-p-sulphinate and iodine yields δ-iodoalkenyl sulphones stereoselectively.These compounds undergo stereospecific dehydrohalogenation to afford dienyl sulphones and nucleophilic

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