3-CHLORO-7-[2-(5-METHYL-3,4-DIOXOCYCLOHEXA-1,5-DIENYLAMINO)-2-PHENYL-ACETYLAMINO]-8-OXO-5-AZABICYCLO-[4.2.0]-OCT-3-ENE-4-CARBOXYLIC-ACID
Compound with spectra: 1 NMR
![3-CHLORO-7-[2-(5-METHYL-3,4-DIOXOCYCLOHEXA-1,5-DIENYLAMINO)-2-PHENYL-ACETYLAMINO]-8-OXO-5-AZABICYCLO-[4.2.0]-OCT-3-ENE-4-CARBOXYLIC-ACID](/api/compound/FSFHildb6ed.png?ph=true&h=300&w=458 "3-CHLORO-7-[2-(5-METHYL-3,4-DIOXOCYCLOHEXA-1,5-DIENYLAMINO)-2-PHENYL-ACETYLAMINO]-8-OXO-5-AZABICYCLO-[4.2.0]-OCT-3-ENE-4-CARBOXYLIC-ACID")
| SpectraBase Compound ID | FSFHildb6ed |
|---|---|
| InChI | InChI=1S/C23H20ClN3O6/c1-11-9-13(10-16(28)20(11)29)25-17(12-5-3-2-4-6-12)21(30)26-18-15-8-7-14(24)19(23(32)33)27(15)22(18)31/h2-6,9-10,15,17-18,25H,7-8H2,1H3,(H,26,30)(H,32,33)/t15-,17-,18+/m1/s1 |
| InChIKey | YKTMAFPTZOKQSY-NXHRZFHOSA-N |
| Mol Weight | 469.88 g/mol |
| Molecular Formula | C23H20ClN3O6 |
| Exact Mass | 469.104063 g/mol |
| Enantiomer InChIKey | YKTMAFPTZOKQSY-RYQLBKOJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
7-[2-(5-METHYL-3,4-DIOXOCYCLOHEXA-1,5-DIENYLAMINO)-2-(4-HYDROXY-PHENYL)-ACETYLAMINO]-CEPHALOSPORANIC-ACID
3-Hydroxy-5-(3-methoxyphenyl)-1-phenethyl-4-(2-thenoyl)-3-pyrrolin-2-one
Cefotaxime anion
(8R,9S,10S,13S,14S)-10,13-Dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carboxylic acid acetyl-amide
Cefixime, trihydrate
sodium 7-({[4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl]carbonyl}amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
Dimethyl 13-isopropyl-8-hydroxy-12-methoxy-7,8-secopodocarpa-8,11,13-triene-7,19-dioate
5-(3,4-dichlorophenyl)-1-[3-(dimethylamino)propyl]-3-hydroxy-4-(2-thienylcarbonyl)-1,5-dihydro-2H-pyrrol-2-one
Punaglandin-4 - epoxide
7-{[(1-ethyl-4-nitro-1H-pyrazol-3-yl)carbonyl]amino}-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
| Title | Journal or Book | Year |
|---|---|---|
| Novel .BETA.-Lactam Antibiotics Synthesized by Amination of Catechols Using Fungal Laccase | Chemical and Pharmaceutical Bulletin | 2008 |