7175-49-7 Usage
Description
N-Ethyldicyclohexylamine is a clear colorless liquid that is utilized in the synthesis of various products, including F-amines. It is formed through a process involving incomplete fluorination and fragmentation reactions, making it a valuable compound in the chemical industry.
Uses
Used in Chemical Synthesis:
N-Ethyldicyclohexylamine is used as a chemical intermediate for the synthesis of F-amines and other products. Its unique structure and properties allow it to participate in various chemical reactions, contributing to the formation of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-Ethyldicyclohexylamine is used as a building block for the development of new drugs. Its versatility in chemical reactions enables the creation of diverse molecular structures with potential therapeutic applications.
Used in Material Science:
N-Ethyldicyclohexylamine is also employed in material science, where it can be used to develop new materials with specific properties. Its ability to undergo various chemical reactions allows for the creation of materials with tailored characteristics for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7175-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7175-49:
(6*7)+(5*1)+(4*7)+(3*5)+(2*4)+(1*9)=107
107 % 10 = 7
So 7175-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H27N/c1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h13-14H,2-12H2,1H3/p+1
7175-49-7Relevant 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.
