2',3'-O-ISOPROPYLIDENE-5'-O-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE
Compound with spectra: 1 NMR
![2',3'-O-ISOPROPYLIDENE-5'-O-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE](/api/compound/AFWC1Ww0Muu.png?ph=true&h=300&w=458 "2',3'-O-ISOPROPYLIDENE-5'-O-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE")
| SpectraBase Compound ID | AFWC1Ww0Muu |
|---|---|
| InChI | InChI=1S/C21H31N5O6/c1-21(2)31-16-13(10-27-7-5-9-29-14-6-3-4-8-28-14)30-20(17(16)32-21)26-12-25-15-18(22)23-11-24-19(15)26/h11-14,16-17,20H,3-10H2,1-2H3,(H2,22,23,24)/t13-,14?,16-,17-,20-/m0/s1 |
| InChIKey | JZIPETLOECLSNX-HCSDNUPTSA-N |
| Mol Weight | 449.51 g/mol |
| Molecular Formula | C21H31N5O6 |
| Exact Mass | 449.227434 g/mol |
| Enantiomer InChIKey | JZIPETLOECLSNX-NWHUNKFXSA-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-(TETRAHYDRO-2H-PYRAN-2-YL)-PENTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[4-(TETRAHYDRO-2H-PYRAN-2-YL)-BUTYL]-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
5'-O-(3-HYDROXYPROPYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(4-HYDROXYBUTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(5-HYDROXYPENTYL)-2',3'-ISOPROPYLIDENE-ADENOSINE
5'-O-(7-HYDROXYHEPTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(6-HYDROXYETHYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[6-[(TOL-4-YL)-SULFONYLOXY]-HEXYL]-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 |