(3RS,4RS)-1-(4-METHOXYPHENYL)-4-METHYL-3-PHTALIMIDE-4-(2-THIENYL)-AZETIDIN-2-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 2xBeDpFWciJ |
|---|---|
| InChI | InChI=1S/C23H18N2O4S/c1-23(18-8-5-13-30-18)19(22(28)25(23)14-9-11-15(29-2)12-10-14)24-20(26)16-6-3-4-7-17(16)21(24)27/h3-13,19H,1-2H3/t19-,23-/m1/s1 |
| InChIKey | HYMKMZHPXBCEOT-AUSIDOKSSA-N |
| Mol Weight | 418.47 g/mol |
| Molecular Formula | C23H18N2O4S |
| Exact Mass | 418.098728 g/mol |
| Enantiomer InChIKey | HYMKMZHPXBCEOT-CVDCTZTESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-(4,6-dimethyl-1,3-benzothiazol-2-yl)-4-(4-ethoxybenzoyl)-5-(4-fluorophenyl)-3-hydroxy-1,5-dihydro-2H-pyrrol-2-one
ethyl 2-({[3-chloro-5-phenyl-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl]carbonyl}amino)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
RU2(MY-O)(MY-O2CCH3)(4-PIC)4(DMSO-D6)2(PF6)2
9-Acetyl-2-chloro-3-phenyl-4-trimethylsilyl-9H-pyrido[2,3-b]indole
3-ALPHA-NONAFLUOROBUTYL-ANDROST-4-EN-3-BETA,17-BETA-DIOL
oxazolo[4,3-a]isoquinolin-3-one, 1-ethyl-1,5,6,10b-tetrahydro-8,9-dimethoxy-1,10b-dimethyl-
Spiro-lingshuiolide
2H-benzo[f]oxireno[2,3-e]benzofuran-8(9H)-one, 9-[[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]methyl]octahydro-2,5a-dimethyl-
Benzo[g]pyridazino[1,2-b]phthalazine-6,13-dione, 2-bromo-1-ethoxy-1,2,3,4-tetrahydro-2,3-dimethyl-, (1.alpha.,2.beta.,3.beta.)-
| Title | Journal or Book | Year |
|---|---|---|
| Staudinger Reaction of Schiff Bases of Acetylthiophene and Acetylpyridine with Ketenes. Diastereoselective Synthesis of 4-Heterosubstituted β-Lactams and their Conversion to β-Thiolactams | Monatshefte für Chemie - Chemical Monthly | 2007 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.