2754-11-2 Usage
Uses
Used in Polymerization Reactions:
4-Ethylmorpholine 4-oxide is used as a catalyst for promoting the process of polymerization, enhancing the efficiency and speed of the reaction.
Used in Pharmaceutical and Agrochemical Industries:
In the pharmaceutical and agrochemical sectors, 4-Ethylmorpholine 4-oxide serves as a component, contributing to the formulation and synthesis of various products.
Used in Organic Synthesis:
As a strong base, 4-Ethylmorpholine 4-oxide is utilized as a reagent in organic synthesis, facilitating specific chemical reactions and transformations.
Used as a Solvent in Various Applications:
4-Ethylmorpholine 4-oxide is employed as a solvent for resins, dyes, and waxes, leveraging its ability to dissolve a range of substances.
Used in Metalworking Fluids:
In the metalworking industry, 4-Ethylmorpholine 4-oxide is used as a corrosion inhibitor, protecting metal surfaces from degradation and wear.
It is crucial to handle 4-Ethylmorpholine 4-oxide with care due to its strong irritant properties, which can cause skin, eye, and respiratory system irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 2754-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2754-11:
(6*2)+(5*7)+(4*5)+(3*4)+(2*1)+(1*1)=82
82 % 10 = 2
So 2754-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-2-7(8)3-5-9-6-4-7/h2-6H2,1H3
2754-11-2Relevant articles and documents
Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid
Gupta, Surabhi,Sureshbabu, Popuri,Singh, Adesh Kumar,Sabiah, Shahulhameed,Kandasamy, Jeyakumar
supporting information, p. 909 - 913 (2017/02/15)
A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies.
