2',3'-O-ISOPROPYLIDENE-5'-O-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-ADENOSINE
Compound with spectra: 1 NMR
![2',3'-O-ISOPROPYLIDENE-5'-O-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-ADENOSINE](/api/compound/6Sq4n8lykqx.png?ph=true&h=300&w=458 "2',3'-O-ISOPROPYLIDENE-5'-O-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-ADENOSINE")
| SpectraBase Compound ID | 6Sq4n8lykqx |
|---|---|
| InChI | InChI=1S/C27H37N5O7S/c1-18-9-11-19(12-10-18)40(33,34)36-14-8-6-4-5-7-13-35-15-20-22-23(39-27(2,3)38-22)26(37-20)32-17-31-21-24(28)29-16-30-25(21)32/h9-12,16-17,20,22-23,26H,4-8,13-15H2,1-3H3,(H2,28,29,30)/t20-,22-,23-,26-/m0/s1 |
| InChIKey | LGJFXXSQRHKTGS-SZBRSHHCSA-N |
| Mol Weight | 575.7 g/mol |
| Molecular Formula | C27H37N5O7S |
| Exact Mass | 575.24137 g/mol |
| Enantiomer InChIKey | LGJFXXSQRHKTGS-HUBRGWSESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2',3'-O-ISOPROPYLIDENE-5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[4-[(TOL-4-YL)-SULFONYLOXY]-BUTYL]-ADENOSINE
5'-O-(7-HYDROXYHEPTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(6-HYDROXYETHYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(5-HYDROXYPENTYL)-2',3'-ISOPROPYLIDENE-ADENOSINE
5'-O-(4-HYDROXYBUTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[7-(TETRAHYDRO-2H-PYRAN-2-YL)-HEPTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[6-(TETRAHYDRO-2-H-PYRAN-2-YL)-HEXYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[5-(TETRAHYDRO-2H-PYRAN-2-YL)-PENTYL]-ADENOSINE
5'-O-(3-HYDROXYPROPYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and Characterization of (5′-Deoxyadenosin-5′-yl)cobalamin ( = ‘Adenosylcobalamin’) Analogues Mimicking the Transition-State Geometry of Coenzyme-B12-Dependent Rearrangements | Helvetica Chimica Acta | 1993 |