91557-33-4 Usage
Uses
Used in Pharmaceutical Industry:
(1Z)-2-morpholin-4-yl-1-phenylethanone oxime is used as a reagent and intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
(1Z)-2-morpholin-4-yl-1-phenylethanone oxime is used as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its ability to chelate metal ions can contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Dye Industry:
(1Z)-2-morpholin-4-yl-1-phenylethanone oxime is used as a precursor in the synthesis of dyes, which can be employed in various applications such as textiles, plastics, and printing inks.
Used in Chelating Agents:
(1Z)-2-morpholin-4-yl-1-phenylethanone oxime is used as a chelating agent, which can bind to metal ions and form stable complexes. This property can be utilized in various applications, such as water treatment, metal extraction, and the synthesis of metal-organic frameworks.
Used in Anti-inflammatory and Neuroprotective Applications:
(1Z)-2-morpholin-4-yl-1-phenylethanone oxime is used as a potential therapeutic agent with anti-inflammatory and neuroprotective properties. Its ability to modulate inflammatory pathways and protect neurons from damage makes it a promising candidate for the treatment of various inflammatory and neurodegenerative disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 91557-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,5 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91557-33:
(7*9)+(6*1)+(5*5)+(4*5)+(3*7)+(2*3)+(1*3)=144
144 % 10 = 4
So 91557-33-4 is a valid CAS Registry Number.
91557-33-4Relevant academic research and scientific papers
Isocyanide-mediated multicomponent synthesis of C-oximinoamidines
Mercalli, Valentina,Meneghetti, Fiorella,Tron, Gian Cesare
, p. 5902 - 5905 (2013/12/04)
By capitalizing on the different reactivity of nitrile N-oxides with isocyanides and amine, α-oximinoamidines, a so far elusive class of compounds, have been synthesized in a straightforward way by reacting isocyanides, syn-chlorooximes, and amines in a multicomponent fashion.
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.
