CAS 84280-59-1
:ethyl 4-methyl-5-oxo-2,5-dihydro-1,2-oxazole-3-carboxylate
Description:
Ethyl 4-methyl-5-oxo-2,5-dihydro-1,2-oxazole-3-carboxylate, with the CAS number 84280-59-1, is a chemical compound characterized by its oxazole ring structure, which contributes to its unique reactivity and properties. This compound features a carboxylate functional group, enhancing its solubility in polar solvents and making it suitable for various chemical reactions. The presence of the ethyl ester group provides it with a degree of volatility and reactivity, often utilized in organic synthesis. Additionally, the methyl and oxo substituents on the oxazole ring can influence its biological activity and potential applications in pharmaceuticals or agrochemicals. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions, although it should be handled with care due to potential reactivity. Its specific applications and behavior in reactions can vary based on the conditions and the presence of other reagents. Overall, this compound is of interest in synthetic organic chemistry and may serve as a building block for more complex molecules.
Formula:C7H9NO4
InChI:InChI=1/C7H9NO4/c1-3-11-7(10)5-4(2)6(9)12-8-5/h8H,3H2,1-2H3
SMILES:CCOC(=O)c1c(C)c(=O)o[nH]1
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Found 3 products.
3-Isoxazolecarboxylicacid, 2,5-dihydro-4-methyl-5-oxo-, ethyl ester
CAS:Formula:C7H9NO4Purity:95%Molecular weight:171.1507ETHYL 4-METHYL-5-OXO-2,5-DIHYDROISOXAZOLE-3-CARBOXYLATE
CAS:Formula:C7H9NO4Purity:95.0%Molecular weight:171.152ethyl 4-methyl-5-oxo-2,5-dihydro-1,2-oxazole-3-carboxylate
CAS:<p>Ethyl 4-methyl-5-oxo-2,5-dihydro-1,2-oxazole-3-carboxylate is a synthetic compound. It can be obtained through the reaction of phthalimido with carbodiimide and esterification of the resultant urea with acetone. The chemical has been used in the synthesis of oxazoles.</p>Formula:C7H9NO4Purity:Min. 95%Molecular weight:171.15 g/mol


