90892-97-0 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(4-methyl-2-oxazolyl)(9CI) serves as a valuable intermediate in organic synthesis, acting as a building block for the creation of more complex organic molecules. Its unique structure, which includes a ketone group and an oxazole ring, allows for versatile chemical reactions, making it a preferred choice for synthesizing a variety of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethanone, 1-(4-methyl-2-oxazolyl)(9CI) is employed as a key component in the development of new drugs. Its chemical properties and reactivity enable the design and synthesis of potential therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
Ethanone, 1-(4-methyl-2-oxazolyl)(9CI) is also utilized in chemical research to study the properties and reactions of ketone derivatives and oxazole-containing compounds. Its use in research helps to expand the understanding of chemical behavior and fosters the discovery of new applications and reactions involving similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 90892-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90892-97:
(7*9)+(6*0)+(5*8)+(4*9)+(3*2)+(2*9)+(1*7)=170
170 % 10 = 0
So 90892-97-0 is a valid CAS Registry Number.
90892-97-0Relevant academic research and scientific papers
Synthesis and Carbodemetalation Reactions of 4-Methyl- and 5-Aryl-2-(trimethylsilyl)oxazoles. C-C Bond Formation at C2 of the Oxazole Ring
Dondoni, Alessandro,Fantin, Giancarlo,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola
, p. 3413 - 3420 (2007/10/02)
The title compounds 6a-d have been prepared by sequential lithiation and silylation of the corresponding 2-H oxazoles and isomerization of the resulting α-isocyano silyl enol ethers.Silyloxazoles 6a-d behave as stable 2-oxazolyl anion equivalents toward v
Intramolecular Insertion of the Isonitrile Group into an Oxygen-Silicon Bond. Synthesis of a 2-Trimethylsilyloxazole via the α-Isocyano Silyl Enol Ether
Dondoni, Alessandro,Dall'Occo, Tiziano,Fantin, Giancarlo,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola
, p. 258 - 260 (2007/10/02)
Treatment of lithiated 4-methyloxazole (1b) with trimethylsilyl chloride gives the α-isocyano silyl enol ether (4b) which when heated in the presence of potassium hydroxide undergoes ring closure to the 2-trimethylsilyloxazole (5b) whose reactions with C-
