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Benzene, 1-(ethenylsulfonyl)-2-methyl-, also known as 2-methyl-1-(ethenylsulfonyl)benzene or 2-methylbenzene-1-sulfonylethylene, is an organic compound with the chemical formula C9H10O2S. It is a colorless liquid with a molecular weight of 182.24 g/mol. Benzene, 1-(ethenylsulfonyl)-2-methyl- is characterized by a benzene ring with a methyl group at the 2-position and an ethenylsulfonyl group at the 1-position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and insecticides. Due to its reactivity and potential applications, it is important to handle this chemical with care, adhering to proper safety protocols.

5535-54-6

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5535-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5535-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5535-54:
(6*5)+(5*5)+(4*3)+(3*5)+(2*5)+(1*4)=96
96 % 10 = 6
So 5535-54-6 is a valid CAS Registry Number.

5535-54-6Relevant academic research and scientific papers

Metal-free visible-light-promoted C(sp3)-H functionalization of aliphatic cyclic ethers using trace O2

Blackburn, Bryan G.,Cooke, Maria Victoria,Laulhé, Sébastien,Niu, Ben,Sachidanandan, Krishnakumar

supporting information, p. 9454 - 9459 (2021/12/09)

Presented is a light-promoted C-C bond forming reaction yielding sulfone and phosphate derivatives at room temperature in the absence of metals or photoredox catalyst. This transformation proceeds in neat conditions through an auto-oxidation mechanism which is maintained through the leaching of trace amounts of O2 as sole green oxidant. This journal is

Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions

Hock, Katharina J.,Mertens, Lucas,Metze, Friederike K.,Schmittmann, Clemens,Koenigs, Rene M.

supporting information, p. 905 - 909 (2017/08/14)

Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.

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