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N-(4-methoxyphenyl)-2,4,6-trimethylbenzamide is a chemical compound with the molecular formula C17H19NO2. It is a derivative of benzamide, featuring a 4-methoxyphenyl group attached to the nitrogen atom and a 2,4,6-trimethylbenzene ring. N-(4-methoxyphenyl)-2,4,6-trimethylbenzamide is known for its potential applications in pharmaceuticals and organic synthesis, particularly as an intermediate in the synthesis of various drugs and agrochemicals. Its structure provides a balance of lipophilicity and polarity, which can influence its solubility and bioavailability. The compound's properties, such as its melting point, boiling point, and solubility, can vary depending on the specific conditions and its purity. N-(4-methoxyphenyl)-2,4,6-trimethylbenzamide is typically synthesized through a series of chemical reactions and is subject to various analytical techniques to confirm its structure and purity.

5215-48-5

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5215-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5215-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5215-48:
(6*5)+(5*2)+(4*1)+(3*5)+(2*4)+(1*8)=75
75 % 10 = 5
So 5215-48-5 is a valid CAS Registry Number.

5215-48-5Downstream Products

5215-48-5Relevant academic research and scientific papers

Synthesis of Secondary Amides from Thiocarbamates

Mampuys, Pieter,Ruijter, Eelco,Orru, Romano V. A.,Maes, Bert U. W.

supporting information, p. 4235 - 4239 (2018/07/29)

The synthesis of secondary amides from readily accessible and bench-stable substituted S-phenyl thiocarbamates and Grignard reactants is reported. Oxidative workup allows recycling of the thiolate leaving group as diphenyl disulfide. Diphenyl disulfide can be transformed into S-phenyl benzenethiosulfonate, a reactant required for thiocarbamate synthesis. This amide synthesis is suitable for the preparation of challenging amides that are not or hardly accessible via classical approaches.

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