69891-38-9 Usage
Uses
Used in Pharmaceutical Industry:
N-CINNAMOYL-N-(2,3-XYLYL)HYDROXYLAMINE is used as an intermediate for the synthesis of various pharmaceuticals due to its reactive aldehyde group, which can be utilized in the formation of new chemical entities with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, N-CINNAMOYL-N-(2,3-XYLYL)HYDROXYLAMINE is employed as an intermediate in the development of agrochemicals, contributing to the creation of compounds that can enhance crop protection and yield.
Used in Dye Industry:
N-CINNAMOYL-N-(2,3-XYLYL)HYDROXYLAMINE is used as an intermediate in the production of dyes, where its chemical properties allow for the creation of a variety of colorants used in different industries such as textiles, plastics, and printing.
Used in Polymer Industry:
As an aldehyde, N-CINNAMOYL-N-(2,3-XYLYL)HYDROXYLAMINE is used as a cross-linking agent in polymers, enhancing their properties and performance in various applications by forming covalent bonds between polymer chains.
Check Digit Verification of cas no
The CAS Registry Mumber 69891-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69891-38:
(7*6)+(6*9)+(5*8)+(4*9)+(3*1)+(2*3)+(1*8)=189
189 % 10 = 9
So 69891-38-9 is a valid CAS Registry Number.
69891-38-9Relevant academic research and scientific papers
Redox-Neutral Selenium-Catalysed Isomerisation of para-Hydroxamic Acids into para-Aminophenols
Chuang, Hsiang-Yu,Schupp, Manuel,Meyrelles, Ricardo,Maryasin, Boris,Maulide, Nuno
, p. 13778 - 13782 (2021/03/31)
A selenium-catalysed para-hydroxylation of N-aryl-hydroxamic acids is reported. Mechanistically, the reaction comprises an N?O bond cleavage and consecutive selenium-induced [2,3]-rearrangement to deliver para-hydroxyaniline derivatives. The mechanism is studied through both 18O-crossover experiments as well as quantum chemical calculations. This redox-neutral transformation provides an unconventional synthetic approach to para-aminophenols.
