90892-99-2 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 4-METHYLOXAZOLE-2-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs. Its chemical properties make it a versatile component in medicinal chemistry, facilitating the creation of compounds with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, ETHYL 4-METHYLOXAZOLE-2-CARBOXYLATE serves as a starting material for the production of crop protection agents. Its incorporation aids in the development of compounds designed to protect crops from pests and diseases, thereby enhancing agricultural productivity.
Used in Research and Development:
ETHYL 4-METHYLOXAZOLE-2-CARBOXYLATE is utilized as a fundamental component in the research and development of innovative pharmaceutical products. Its presence in experimental formulations allows scientists to explore new avenues in drug discovery and design.
Used in Production of Fine Chemicals:
ETHYL 4-METHYLOXAZOLE-2-CARBOXYLATE is also used in the manufacturing process of fine chemicals, which are crucial for various industrial applications. Its role in this context is to provide a stable and reactive platform for the synthesis of high-quality specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 90892-99-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 90892-99:
(7*9)+(6*0)+(5*8)+(4*9)+(3*2)+(2*9)+(1*9)=172
172 % 10 = 2
So 90892-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-3-10-7(9)6-8-5(2)4-11-6/h4H,3H2,1-2H3
90892-99-2Relevant 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-
