#12;N-[(1R,2R)-1-[[BIS-(4-METHOXYPHENYL)-PHENYLMETHOXY]-METHYL]-2-[2-CYANOETHOXYDIISOPROPYLAMINO)-PHOSPHANYL]-OXYPROPYL]-4-(DITHIOLAN-3-YL)-BUTANAMIDE
Compound with spectra: 1 NMR
![#12;N-[(1R,2R)-1-[[BIS-(4-METHOXYPHENYL)-PHENYLMETHOXY]-METHYL]-2-[2-CYANOETHOXYDIISOPROPYLAMINO)-PHOSPHANYL]-OXYPROPYL]-4-(DITHIOLAN-3-YL)-BUTANAMIDE](/api/compound/7HBuYxHTHHE.png?ph=true&h=300&w=458 "#12;N-[(1R,2R)-1-[[BIS-(4-METHOXYPHENYL)-PHENYLMETHOXY]-METHYL]-2-[2-CYANOETHOXYDIISOPROPYLAMINO)-PHOSPHANYL]-OXYPROPYL]-4-(DITHIOLAN-3-YL)-BUTANAMIDE")
| SpectraBase Compound ID | 7HBuYxHTHHE |
|---|---|
| InChI | InChI=1S/C42H58N3O6PS2/c1-31(2)45(32(3)4)52(50-28-13-27-43)51-33(5)40(44-41(46)17-12-11-16-39-26-29-53-54-39)30-49-42(34-14-9-8-10-15-34,35-18-22-37(47-6)23-19-35)36-20-24-38(48-7)25-21-36/h8-10,14-15,18-25,31-33,39-40H,11-13,16-17,26,28-30H2,1-7H3,(H,44,46)/t33-,39?,40-,52?/m1/s1 |
| InChIKey | HGUICGJOPVKELG-NAWMBHOSSA-N |
| Mol Weight | 796.0 g/mol |
| Molecular Formula | C42H58N3O6PS2 |
| Exact Mass | 795.350466 g/mol |
| Enantiomer InChIKey | HGUICGJOPVKELG-JZALPFEASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
QZJFOTQODZNZPH-OJDZSJEKSA-N
TERT.-BUTYLOXYCARBONYL-N-(6-O-(4-METHOXYTRITYL)-BETA-D-GLUCOPYRANOSYL)-METHYLAMINE
N-(TERT.-BUTOXYCARBONYL)-[6-O-(4-METHOXYTRITYL)-BETA-D-GALACTOPYRANOSYL]-METHYLAMINE
1-((1R,3S)-TETRAHYDRO-3-(((4-METHOXYPHENYL)-DIPHENYLMETHOXY)-METHYL)-1-FURANYL)-2,4(1H,3H)-PYRIMIDINEDIONE
(-)-TERT.-BUTYL-(2S,3R)-3-HYDROXY-6-OXO-2-[(TRITYLOXY)-METHYL]-3,6-DIHYDROPYRIDIN-1(2H)-CARBOXYLATE
(+/-)-1ALPHA-[6-METHOXYCARBONYLHEX-2Z-ENYL]-2BETA-TRIPHENYLMETHOXYMETHYL-3ALPHA,5ALPHA-DIACETOXYCYCLOPENTANE
1-(2,3-DI-O-BENZYL-6-O-TRITYL-L-ARABINOFURANOSYL)-ACETONE
Methyl 4-O-(Diethyl phosphonoacetyl)-2,3-dideoxy-2-C-methyl-6-O-triphenylmethyl-.alpha.-D-arabino-hexopyranoside
3-BENZOYL-2-STEAROYL-RAC-SFINGANIN-1-(N-TRIPHENYLMETHYLAMINOETHYL)PHOSPHATE
Phenolphthalein 2ME
| Title | Journal or Book | Year |
|---|---|---|
| Thioctic Acid Derivatives as Building Blocks to Incorporate DNA Oligonucleotides onto Gold Nanoparticles | Molecules | 2014 |