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4-Acetyl-benzolsulfonsaeure-phenylester, also known as 4-acetylphenyl phenyl sulfone, is an organic compound with the chemical formula C14H12O3S. It is a derivative of benzene, featuring a phenyl group (C6H5), a 4-acetyl group (CH3CO), and a sulfone group (SO2). 4-Acetyl-benzolsulfonsaeure-phenylester is characterized by its aromatic structure and the presence of a sulfone functional group, which contributes to its chemical reactivity and stability. It is used in various chemical synthesis processes, particularly in the production of pharmaceuticals and other organic compounds. The compound's properties, such as its solubility and reactivity, make it a valuable intermediate in the synthesis of more complex molecules.

4574-68-9

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4574-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4574-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,7 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4574-68:
(6*4)+(5*5)+(4*7)+(3*4)+(2*6)+(1*8)=109
109 % 10 = 9
So 4574-68-9 is a valid CAS Registry Number.

4574-68-9Relevant academic research and scientific papers

Quantum Dot-Catalyzed Photoreductive Removal of Sulfonyl-Based Protecting Groups

Perez, Kaitlyn A.,Rogers, Cameron R.,Weiss, Emily A.

, p. 14091 - 14095 (2020)

This Communication describes the use of CuInS2/ZnS quantum dots (QDs) as photocatalysts for the reductive deprotection of aryl sulfonyl-protected phenols. For a series of aryl sulfonates with electron-withdrawing substituents, the rate of deprotection for the corresponding phenyl aryl sulfonates increases with decreasing electrochemical potential for the two electron transfers within the catalytic cycle. The rate of deprotection for a substrate that contains a carboxylic acid, a known QD-binding group, is accelerated by more than a factor of ten from that expected from the electrochemical potential for the transformation, a result that suggests that formation of metastable electron donor–acceptor complexes provides a significant kinetic advantage. This deprotection method does not perturb the common NHBoc or toluenesulfonyl protecting groups and, as demonstrated with an estrone substrate, does not perturb proximate ketones, which are generally vulnerable to many chemical reduction methods used for this class of reactions.

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