15437-09-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
(1E)-2-morpholin-4-yl-1-phenylethanone oxime is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used as a Chelating Agent:
(1E)-2-morpholin-4-yl-1-phenylethanone oxime serves as a chelating agent, which is employed in the production of metal complexes. Its ability to form stable complexes with metal ions is valuable in various chemical processes and applications.
Used in Antiviral, Antifungal, and Antibacterial Applications:
(1E)-2-morpholin-4-yl-1-phenylethanone oxime has been studied for its potential biological activities, including antiviral, antifungal, and antibacterial properties. These characteristics make it a promising candidate for use in the development of treatments and preventive measures against a range of infectious diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 15437-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,3 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15437-09:
(7*1)+(6*5)+(5*4)+(4*3)+(3*7)+(2*0)+(1*9)=99
99 % 10 = 9
So 15437-09-9 is a valid CAS Registry Number.
15437-09-9Relevant academic research and scientific papers
STEREOCHEMISTRY OF α-AMINOACETOPHENONE OXIMES STUDY OF SOLVENT EFFECTS
Moehrle, H.,Wehefritz, B.,Steigel, A.
, p. 2255 - 2260 (2007/10/02)
The aminolysis of Z-α-halogenoacetophenone oximes results in different mixtures of E- and Z-α-aminoacetophenone oximes depending on the solvent used.Assignment of configuration can be achieved by 13C NMR spectroscopy even if only one isomer is available using a strong solvent dependence of the methylene chemical shift in the case of the Z-isomers.This effect is due to the presence of different conformations in the solvents chloroform and dimethyl sulfoxide.Together with a study by vapor pressure osmometry the results provide an unambiguous proof of intramolecular hydrogen bonding of Z-α-aminoacetophenone oximes in chloroform.
