N-(carbethoxyamino)-N-[[4-(4,4-dimethyl-5H-oxazol-2-yl)-3-methyl-isoxazol-5-yl]methyl]carbamic acid ethyl ester
Compound with spectra: 1 NMR
![N-(carbethoxyamino)-N-[[4-(4,4-dimethyl-5H-oxazol-2-yl)-3-methyl-isoxazol-5-yl]methyl]carbamic acid ethyl ester](/api/compound/82QDVA1Gzo4.png?ph=true&h=300&w=458 "N-(carbethoxyamino)-N-[[4-(4,4-dimethyl-5H-oxazol-2-yl)-3-methyl-isoxazol-5-yl]methyl]carbamic acid ethyl ester")
| SpectraBase Compound ID | 82QDVA1Gzo4 |
|---|---|
| InChI | InChI=1S/C16H24N4O6/c1-6-23-14(21)18-20(15(22)24-7-2)8-11-12(10(3)19-26-11)13-17-16(4,5)9-25-13/h6-9H2,1-5H3,(H,18,21) |
| InChIKey | HREHQCPLXAVGHV-UHFFFAOYSA-N |
| Mol Weight | 368.39 g/mol |
| Molecular Formula | C16H24N4O6 |
| Exact Mass | 368.169585 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
4-(4,4-Dimethyl-4,5-dihydro-2-oxazolinyl)-3-phenyl-5-(phenylthiomethyl)isoxazole
12H-7,11-Nitrilo-6H-dibenzo[b,k][1,4,7,10,13]pentaoxacycloeicosin, 8-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-19,20,22,23-tetrahydro-
trans-2-(p-METHYLSTYRYL)-3-PHENYL-4(3H)-QUINAZOLINONE
trans-2-[2-(4-Dimethylaminophenyl)vinyl]-3-phenyl-3H-quinazolin-4-one[new2]2-[(E)-2-(4-Dimethylamino-phenyl)-vinyl]-3-phenyl-3H-quinazolin-4-one
5-Phenyl-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-8(9H)-one
2-[(E)-2-(4-Fluoro-phenyl)-vinyl]-3-phenyl-3H-quinazolin-4-one
Diethyl (R)-1-(1-methoxy-1-oxo-2-(4'-(trifluoromethyl)biphenyl-4-yl)propan-2-yl)hydrazine-1,2-dicarboxylate
1-((2-[(2,4-Dichlorobenzoyl)oxy]-1-naphthyl)methyl)-2-naphthyl 2,4-dichlorobenzoate
Diethyl (R)-1-(2-(biphenyl-4-yl)-1-methoxy-1-oxopropan-2-yl)hydrazine-1,2-dicarboxylate
3-Phenyl-2-((E)-styryl)-3H-quinazolin-4-one
| Title | Journal or Book | Year |
|---|---|---|
| Selective lateral metalation and electrophilic quenching of c-4 functionalized isoxazoles.IX. Direct formation of the C-N bond utilizing an electrophilic nitrogen source | Journal of Heterocyclic Chemistry | 1990 |