53064-41-8 Usage
Description
Ethyl 3-ethyl-5-methyl-4-isoxazolecarboxylate is an organic compound that serves as a valuable intermediate in the synthesis of various chemical compounds. It is characterized by its unique molecular structure, which includes an isoxazole ring and an ester functional group.
Uses
Used in Pharmaceutical Industry:
Ethyl 3-ethyl-5-methyl-4-isoxazolecarboxylate is used as an intermediate in the synthesis of cyclotetra-methyleneisoxazole, a new analeptic agent. This analeptic is designed to counteract the effects of sedatives and promote wakefulness, making it a potentially important compound in the development of medications for various conditions related to fatigue or sedation.
Used in Chemical Synthesis:
Ethyl 3-ethyl-5-methyl-4-isoxazolecarboxylate is also used as a building block in the preparation of other complex organic molecules. Its unique structure and functional groups make it a versatile component in the synthesis of a wide range of compounds, including those with potential applications in various industries such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 53064-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,6 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53064-41:
(7*5)+(6*3)+(5*0)+(4*6)+(3*4)+(2*4)+(1*1)=98
98 % 10 = 8
So 53064-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO3/c1-4-7-8(6(3)13-10-7)9(11)12-5-2/h4-5H2,1-3H3
53064-41-8Relevant articles and documents
Preparation and rearrangement of N-vinyl nitrones: Synthesis of spiroisoxazolines and fluorene-tethered isoxazoles
Mo, Dong-Liang,Wink, Donald A.,Anderson, Laura L.
supporting information, p. 5180 - 5183,4 (2012/12/12)
N-Vinyl nitrones derived from fluorenone have been prepared via a copper-mediated coupling between fluorenone oxime and vinyl boronic acids. These compounds undergo subsequent rearrangement and addition reactions that are distinct from the traditional [3 + 2] cycloaddition reactivity of nitrones. Thermal rearrangements of fluorenone N-vinyl nitrones give spiroisoxazolines, while treatment with alkynes provides fluorene-tethered isoxazoles. The scope and limitations of the preparation of fluorenone N-vinyl nitrones and their subsequent rearrangement and addition reactions are discussed.
