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1,2-dimethoxy-4-(tosylmethyl)benzene is an organic compound with the molecular formula C11H14O4S. It is a derivative of benzene, featuring two methoxy groups (-OCH3) at the 1st and 2nd carbon positions, and a tosylmethyl group (-CH2-Ts, where Ts represents the tosyl or p-toluenesulfonyl group) at the 4th carbon position. 1,2-dimethoxy-4-(tosylmethyl)benzene is known for its potential applications in organic synthesis, particularly as a precursor in the preparation of various pharmaceuticals and agrochemicals. The presence of the tosylmethyl group makes it a valuable intermediate due to its reactivity and the ability to undergo various chemical transformations, such as nucleophilic substitutions and eliminations. The compound's structure allows for the introduction of different functional groups at the benzene ring, making it a versatile building block in the synthesis of complex molecules.

3795-83-3

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3795-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3795-83-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3795-83:
(6*3)+(5*7)+(4*9)+(3*5)+(2*8)+(1*3)=123
123 % 10 = 3
So 3795-83-3 is a valid CAS Registry Number.

3795-83-3Downstream Products

3795-83-3Relevant academic research and scientific papers

Visible-Light-Catalyzed in Situ Denitrogenative Sulfonylation of Sulfonylhydrazones

Huang, Xiang,Chen, Xing,Xie, Haisheng,Tan, Zheng,Jiang, Huanfeng,Zeng, Wei

, p. 6784 - 6788 (2021/09/08)

A photocatalyzed in situ denitrogenative sulfonylation of N-arylsulfonyl hydrazones has been developed. This transformation provides a low-carbon strategy to assemble arylalkyl sulfones in a stepwise denitrogenation/sulfonylation manner.

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