2',3'-O-ISOPROPYLIDENE-5'-O-[7-(TETRAHYDRO-2H-PYRAN-2-YL)-HEPTYL]-ADENOSINE
Compound with spectra: 1 NMR
![2',3'-O-ISOPROPYLIDENE-5'-O-[7-(TETRAHYDRO-2H-PYRAN-2-YL)-HEPTYL]-ADENOSINE](/api/compound/LhGu4bJsC1f.png?ph=true&h=300&w=458 "2',3'-O-ISOPROPYLIDENE-5'-O-[7-(TETRAHYDRO-2H-PYRAN-2-YL)-HEPTYL]-ADENOSINE")
| SpectraBase Compound ID | LhGu4bJsC1f |
|---|---|
| InChI | InChI=1S/C25H39N5O6/c1-25(2)35-20-17(14-31-11-7-4-3-5-8-12-32-18-10-6-9-13-33-18)34-24(21(20)36-25)30-16-29-19-22(26)27-15-28-23(19)30/h15-18,20-21,24H,3-14H2,1-2H3,(H2,26,27,28)/t17-,18?,20-,21-,24-/m0/s1 |
| InChIKey | KICCXFIOMDMOJY-UAKVJOTFSA-N |
| Mol Weight | 505.6 g/mol |
| Molecular Formula | C25H39N5O6 |
| Exact Mass | 505.290034 g/mol |
| Enantiomer InChIKey | KICCXFIOMDMOJY-UEILJKQYSA-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-[6-(TETRAHYDRO-2-H-PYRAN-2-YL)-HEXYL]-ADENOSINE
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
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-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE
5'-O-(3-HYDROXYPROPYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-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 |