BENZYL-6-ALPHA-[(PARA-TOLUENESULFONYL)-OXY]-PENICILLANATE
Compound with spectra: 1 NMR
![BENZYL-6-ALPHA-[(PARA-TOLUENESULFONYL)-OXY]-PENICILLANATE](/api/compound/17Utl9T4YrI.png?ph=true&h=300&w=458 "BENZYL-6-ALPHA-[(PARA-TOLUENESULFONYL)-OXY]-PENICILLANATE")
| SpectraBase Compound ID | 17Utl9T4YrI |
|---|---|
| InChI | InChI=1S/C22H23NO6S2/c1-14-9-11-16(12-10-14)31(26,27)29-17-19(24)23-18(22(2,3)30-20(17)23)21(25)28-13-15-7-5-4-6-8-15/h4-12,17-18,20H,13H2,1-3H3/t17-,18-,20+/m0/s1 |
| InChIKey | KFQSDSASRAMAJG-CMKODMSKSA-N |
| Mol Weight | 461.55 g/mol |
| Molecular Formula | C22H23NO6S2 |
| Exact Mass | 461.09668 g/mol |
| Enantiomer InChIKey | KFQSDSASRAMAJG-GGPKGHCWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(PIVALOYLOXY)-METHYL-6-ALPHA-[(PARA-TOLUENESULFONYL)-OXY]-PENICILLANATE
BENZYL-6-ALPHA-(DIPHENYL-PHOSPHATE)-OXYPENICILLANATE
BACAMPICILLIN;HYDROCHLORIDE
N-TRIFLUOROMETHYLSULPHENYLPIVAMPICILLIN
6-[[2-[3-[5-[2-[(2-carbomethoxy-7-keto-3,3-dimethyl-4-thia-1-azabicyclo[3.2.0]heptan-6-yl)amino]-2-keto-ethyl]-2-hydroxy-phenyl]-4-hydroxy-phenyl]acetyl]amino]-7-keto-3,3-dimethyl-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid methyl ester
Pivampicillin cation
6-{[2-(p-chlorophenyl)-N-cyanoacetimidoyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3,2,0]heptane-2-carboxylic acid, hydroxymethyl ester, pivalate(ester)
6-[[2-[3-[4-[2-[(2-carbomethoxy-7-keto-3,3-dimethyl-4-thia-1-azabicyclo[3.2.0]heptan-6-yl)amino]-2-keto-ethyl]phenoxy]-4-hydroxy-phenyl]acetyl]amino]-7-keto-3,3-dimethyl-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid methyl ester
6-[(N-cyano-2-phenylacetimidoyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3,2,0]heptane-2-carboxylic acid, hydroxymethyl ester,pivalate(ester)
6-{[(4-chloro-1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
| Title | Journal or Book | Year |
|---|---|---|
| Contributions to the Development of New Substitution Patterns of Penicillins: Synthesis of New Penicillins Derivatives and Evaluation of their Porcine Pancreatic Elastase Inhibitory Activity | Journal Of The Brazilian Chemical Society | 1996 |