OMXILAIFDCNRLP-NRFANRHFSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | KARFgntpzaa |
|---|---|
| InChI | InChI=1S/C22H25N3O2/c1-5-23(6-2)22-16(4)21-20(25(26)27-22)15(3)12-19-13-18(14-24(19)21)17-10-8-7-9-11-17/h7-14,21H,5-6H2,1-4H3/t21-/m0/s1 |
| InChIKey | OMXILAIFDCNRLP-NRFANRHFSA-N |
| Mol Weight | 363.46 g/mol |
| Molecular Formula | C22H25N3O2 |
| Exact Mass | 363.194677 g/mol |
| Enantiomer InChIKey | OMXILAIFDCNRLP-OAQYLSRUSA-N |
| Racemate InChIKey | OMXILAIFDCNRLP-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
1-(2,4-Xylidino)-2-ethyl-3-methylpyrido[1,2-a]benzimidazole-4-carbonitrile
10-.beta.-Hydroxyestr-4-en-3,17-dione Methyloxime-trimethylsilyl dev
(/.eta.-5/-Pentamethyl-cyclopentadienyl)-trimethylphosphino-butyl-hydrido rhodium
N-(1-(Diphenylphosphoryl)-5-methoxy-3-(4-methoxybenzyl)-1H-inden-2-yl)benzamide
N-(1-(Diphenylphosphoryl)-3-(4-fluorobenzyl)-5-methoxy-1H-inden-2-yl)benzamide
1(3H)-ISOBENZOFURANONE, 4-[5-(3-FURANYL)TETRAHYDRO-2,3-DIMETHYLFURO[2,3-b]FURAN-
4,4,6,8-tetramethyl-5-(4-morpholinylacetyl)-4,5-dihydro-1H-[1,2]dithiolo[3,4-c]quinoline-1-thione
12-(4-Tolylsulfonyl)-9,10-dihydro-9,10-etheno-anthracen-11-yl-phosphonic acid, diethyl ester
COROMANDELIN-HEPTAACETATE;PRUNETIN-4'-O-PIOSYL-(->6)-GLUCOSIDE-HEPTAACETATE
8-Hexyl-6-(trimethylsilyl)-8H-indolo[3,2-a]phenazine
| Title | Journal or Book | Year |
|---|---|---|
| Quantum Chemical Analysis and Experimental Study of the Cycloaddition Reaction between Aminoacetylenes and 6-Nitroindolizines. NMR and ab Initio Evidence for the [4+2] Adduct Formation | The Journal of Organic Chemistry | 1999 |
This compound is available in the following databases:
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.