XEKUURUQXMSNAH-UHFFFAOYSA-L
Compound with spectra: 1 NMR
| SpectraBase Compound ID | GjRAD6fj2mT |
|---|---|
| InChI | InChI=1S/C24H36N2O2.CHF3O3S.ClH.Rh/c1-15-9-16(2)18(12-22-26-20(14-28-22)24(6,7)8)10-17(15)11-21-25-19(13-27-21)23(3,4)5;2-1(3,4)8(5,6)7;;/h9-10,19-20H,11-14H2,1-8H3;(H,5,6,7);1H;/q;;;+2/p-2 |
| InChIKey | XEKUURUQXMSNAH-UHFFFAOYSA-L |
| Mol Weight | 672.0 g/mol |
| Molecular Formula | C25H36ClF3N2O5RhS |
| Exact Mass | 671.104046 g/mol |
| Parent InChIKey | TZRCLXVMMWTJQK-UHFFFAOYSA-L |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
ethyl 2-{[[(2E)-2-(4-ethoxybenzylidene)hydrazino](oxo)acetyl]amino}-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxylate
methyl 2-{[{(2E)-2-[3-(2-amino-2-oxoethoxy)benzylidene]hydrazino}(oxo)acetyl]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
4-Methoxycarbonyl-4-(4-methoxyphenyl)-2H-1-benzopyran-3(4H)-one
methyl 2-{[{(2E)-2-[1-(2-hydroxyphenyl)ethylidene]hydrazino}(oxo)acetyl]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
isopropyl 2-{[(3,4-dichlorophenoxy)acetyl]amino}-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxylate
Bornaprine-M (OH) I
Methyl (2R,3S)-rel-1,2,3,4,5,6,7,8-Octahydro-3-(3-methoxyphenyl)-6,6-dimethyl-8-oxo-2-naphthalenecarboxylate
1,7-Dimethoxycarbonyl-6-phenyl-4-oxa-5-azaspiro[2,4]hept-5-ene
ANGELOL_C;6_[(1-R,2-S)-1,3-DIHYDROXY-2-METHYLBUTYRYL]-7-METHOXYCOUMARIN;_SEEREMARK__
(+)-3-BETA,13-DIACETOXYMANOOL
| Title | Journal or Book | Year |
|---|---|---|
| Monomeric Rhodium(II) Catalysts for the Preparation of Aziridines and Enantioselective Formation of Cyclopropanes from Ethyl Diazoacetate at Room Temperature | The Journal of Organic Chemistry | 2003 |
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.