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1-<(4-Methylphenyl)sulfinyl>-3-methyl-2-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123359-08-0

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123359-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123359-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,5 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123359-08:
(8*1)+(7*2)+(6*3)+(5*3)+(4*5)+(3*9)+(2*0)+(1*8)=110
110 % 10 = 0
So 123359-08-0 is a valid CAS Registry Number.

123359-08-0Downstream Products

123359-08-0Relevant academic research and scientific papers

3-silicon based containing 1,2,3,5-tetrasubstituted benzene and synthetic method thereof

-

Paragraph 0019; 0020, (2018/12/13)

The invention discloses a 3-silicon based containing 1,2,3,5-tetrasubstituted benzene synthetized by utilizing a simple aryne precursor containing a silicon group at 3-position and a synthetic methodthereof. A structure is shown as the description. The sy

Aryne 1,2,3-Trifunctionalization with Aryl Allyl Sulfoxides

Li, Yuanyuan,Qiu, Dachuan,Gu, Rongrong,Wang, Junli,Shi, Jiarong,Li, Yang

supporting information, p. 10814 - 10817 (2016/09/12)

An aryne 1,2,3-trisubstitution with aryl allyl sulfoxides is accomplished, featuring an incorporation of C-S, C-O, and C-C bonds on the consecutive positions of a benzene ring. The reaction condition is mild with broad substrate scope. Preliminary mechani

Temperature, Solvent, and Substituent Effects on the Singlet Oxidations of Allylic Phenyl Sulfoxides, Sulfones, and Sulfides

Clennan, Edward L.,Chen, Xiangning

, p. 8212 - 8218 (2007/10/02)

The reaction of singlet oxygen with a series of allylic sulfoxides, sulfones, and sulfides have been examined as a function of extent of reaction, temperature, and solvent.Hydroperoxy groups but not alkyl, hydrogen, or hydroxyl on chiral carbons β to sulfide sulfur induce diastereoselective sulfoxide formations.Evidence is presented that suggests that the oxidation at sulfur occurs with anchimeric assistance from the hydroperoxy group via a favorable sulfurane-like transition state.

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