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Diethyl (N,4-dimethyl-benzenesulfonamide-1-yl)phosphonate is a complex organic compound with the chemical formula C14H22NO4PS. It is a derivative of benzenesulfonamide, featuring a phosphonate group attached to the nitrogen atom. diethyl (N,4-dimethyl-benzenesulfonamide-1-yl)phosphonate is characterized by its two ethyl groups (C2H5), a dimethyl group (CH3)2, and a phosphonate group (PO3H2). It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of certain pesticides. The compound's structure and properties make it a versatile intermediate in organic chemistry, although its specific uses and safety considerations should be carefully evaluated.

7301-63-5

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7301-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7301-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7301-63:
(6*7)+(5*3)+(4*0)+(3*1)+(2*6)+(1*3)=75
75 % 10 = 5
So 7301-63-5 is a valid CAS Registry Number.

7301-63-5Downstream Products

7301-63-5Relevant academic research and scientific papers

Electrochemical Regioselective Phosphorylation of Nitrogen-Containing Heterocycles and Related Derivatives

Deng, Yong,You, Shiqi,Ruan, Mengyao,Wang, Ying,Chen, Zuxing,Yang, Guichun,Gao, Meng

, p. 464 - 469 (2021)

The site-selective functionalization of biologically important nitrogen-containing heterocycles and related derivatives remains a challenging and important task. We report herein on the direct regiodivergent N1/C2 phosphorylation of free indole derivatives. Cyclic voltammograms and EPR data indicate that by utilizing different electrolyte-mediated anodic oxidation to generate different active indole species, a diverse collection of N1 and C2 phosphorylation products could be obtained in moderate to high yields under exogenous-oxidant-free and metal-catalyst-free electrochemical conditions. In addition, N?P coupling was also found to be compatible with various alkylamines. (Figure presented.).

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