76390-72-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethanone, 1-(4-amino-3-phenyl-5-isoxazolyl)is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Compounds Synthesis:
Ethanone, 1-(4-amino-3-phenyl-5-isoxazolyl)serves as a building block in the synthesis of a range of organic compounds, contributing to the advancement of organic chemistry and the creation of novel materials with diverse applications.
Used in Medicinal Research:
Ethanone, 1-(4-amino-3-phenyl-5-isoxazolyl)is being studied for its potential medicinal properties, with ongoing research exploring its use in the treatment of various diseases and conditions. Its unique structure and reactivity make it a promising candidate for the development of new therapeutic agents.
Used in Chemical Research and Development:
Due to its potential applications in various fields, Ethanone, 1-(4-amino-3-phenyl-5-isoxazolyl)is also used in chemical research and development to explore new reactions, mechanisms, and applications, further expanding the scope of its utility in the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 76390-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,9 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76390-72:
(7*7)+(6*6)+(5*3)+(4*9)+(3*0)+(2*7)+(1*2)=152
152 % 10 = 2
So 76390-72-2 is a valid CAS Registry Number.
76390-72-2Relevant academic research and scientific papers
Kislyi,Danilova,Solkan
, p. 1042 - 1054 (2013)
The base-catalyzed cyclization of oximinonitriles in the presence of lithium ions leads to 4-aminoisoxazoles and, sometimes, to 5-aminooxazoles. Modeling using the density functional theory and the HF and MP2 methods indicated that both 4-aminoisoxazoles
4-Aminoisoxazoles by Thorpe Cyclization
Gewald, Karl,Bellmann, Peter,Jaensch, Hans-Joachim
, p. 1623 - 1629 (2007/10/02)
Cyclization of α-(acylmethoxyimino)nitriles 1 in the presence of lithium hydroxide yields 5-acyl-4-aminoisoxazoles 2.Compounds 2f and 2a can be converted into the isoxazolopyrimidone 3 and the isoxazolopyridine 4.
