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2-Methoxy-4-(tosylmethyl)phenol is an organic compound characterized by its molecular formula C15H16O4S. It is a derivative of phenol, with a methoxy group (-OCH3) at the 2-position and a tosylmethyl group (-CH2-Ts, where Ts represents the tosyl or p-toluenesulfonyl group) at the 4-position. 2-methoxy-4-(tosylmethyl)phenol is known for its potential applications in organic synthesis, particularly as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its structure provides a balance of reactivity and stability, making it a valuable building block in the synthesis of more complex molecules. The tosylmethyl group can act as a protecting group or a leaving group in various chemical reactions, while the methoxy group can influence the electronic properties of the aromatic ring.

3795-82-2

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3795-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3795-82-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 3795-82:
(6*3)+(5*7)+(4*9)+(3*5)+(2*8)+(1*2)=122
122 % 10 = 2
So 3795-82-2 is a valid CAS Registry Number.

3795-82-2Relevant academic research and scientific papers

Iron(III) phthalocyanine-chloride-catalyzed synthesis of sulfones from sulfonylhydrazones

Zhao, Jun-Long,Guo, Shi-Huan,Qiu, Jun,Gou, Xiao-Feng,Hua, Cheng-Wen,Chen, Bang

supporting information, p. 2375 - 2378 (2016/05/19)

In this study, sulfones are synthesized from sulfonylhydrazones catalyzed by iron(III) phthalocyanine chloride. This reaction offers broad substrate scope, occurs under mild conditions, utilized readily available reactants, and forms products in good-to-h

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