52913-15-2

Usage

Uses

Used in Pharmaceutical Industry:
N-[[(4-Methylphenyl)sulfonyl]oxy]-ethanimidic acidethylester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its sulfonyl group plays a crucial role in the formation of active pharmaceutical ingredients, contributing to their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, N-[[(4-Methylphenyl)sulfonyl]oxy]-ethanimidic acidethylester serves as an intermediate in the production of various agrochemicals, such as pesticides and herbicides. Its unique chemical structure allows for the development of effective and targeted agrochemicals.
Used in Dye Industry:
N-[[(4-Methylphenyl)sulfonyl]oxy]-ethanimidic acidethylester is utilized as a key intermediate in the synthesis of dyes, particularly those used in the textile and printing industries. Its sulfonyl group contributes to the colorfastness and stability of the dyes, ensuring their performance and longevity.

InChI:InChI=1/C11H15NO4S/c1-4-15-10(3)12-16-17(13,14)11-7-5-9(2)6-8-11/h5-8H,4H2,1-3H3

Upstream product

• 10576-12-2 ethyl acetohydroximate 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 64890-25-1 N-Amino-4-tert-butylpyridinium p-tosylate 
• 52913-14-1 O-tosylhydroxylamine 

Relevant academic research and scientific papers

1,3,4,5-Tetraamino-1,2,4-triazolium Cation: An Energetic Moiety

The amination of 3,4,5-triamino-1,2,4-triazole with O-tosylhydroxylamine yielded the nitrogen-rich 1,3,4,5-tetraamino-1,2,4-triazolium cation as its tosylate salt. Subsequent metathesis reactions produced energetic salts with various energetic anions, inc

O - substituted hydroxylamine hydrochloride and its preparation method (by machine translation)

The present invention provides a O - substituted hydroxylamine hydrochloride and its preparation, wherein the preparation method comprises the following steps: step S1, to the acetyl hydroximic acid ethyl ester in ethanol solution of adding sodium hydroxide, in addition at the same time instillment halohydrocarbon, chloride or acyl chloride substitution reaction to take place, then added to the water in order to separate out the O - substituted [...]; step S2, the said O - substituted [...] adding hydrochloric acid solution in order to produce reflux reaction O - substituted hydroxylamine hydrochloride. According to the embodiment of the invention of the O - substituted hydroxylamine hydrochloride of the preparation method, high purity of the product can be obtained, and the method is safe, easy to process, the process is simple, and is suitable for industrial production. (by machine translation)

Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment 13. Synthesis and profiling of a novel amminium prodrug of the HIV-1 attachment inhibitor BMS-585248

In vitro studies suggested that the ammonium salt 2 could be a viable prodrug of the HIV-1 attachment inhibitor 1. Increased systemic exposure of the parent drug 1 following oral administration of the amminium salt 2 when compared to similar studies using

Weak Interactions in Crystals: 4,4'-Di(tert-butyl)-N-N'-bipyridinium Diperchlorate - A Biphenyl Analogue with Perpendicular Pyridine Rings

Oxidation of substituted N-aminopyridinium compounds yields bipyridinium salts.After anion exchange Br(1-) --> ClO4(1-), it was possible to grow single crystals from the 4,4'-di(tert-butyl)derivative.The structure determined at 100 K shows a dihedral angl