2',3'-O-ISOPROPYLIDENE-5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE
Compound with spectra: 1 NMR
![2',3'-O-ISOPROPYLIDENE-5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE](/api/compound/CuJsiqf2IN9.png?ph=true&h=300&w=458 "2',3'-O-ISOPROPYLIDENE-5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE")
| SpectraBase Compound ID | CuJsiqf2IN9 |
|---|---|
| InChI | InChI=1S/C25H33N5O7S/c1-16-7-9-17(10-8-16)38(31,32)34-12-6-4-5-11-33-13-18-20-21(37-25(2,3)36-20)24(35-18)30-15-29-19-22(26)27-14-28-23(19)30/h7-10,14-15,18,20-21,24H,4-6,11-13H2,1-3H3,(H2,26,27,28)/t18-,20-,21-,24-/m0/s1 |
| InChIKey | ICSUAADVGLPLFO-FVLCUVFVSA-N |
| Mol Weight | 547.6 g/mol |
| Molecular Formula | C25H33N5O7S |
| Exact Mass | 547.21007 g/mol |
| Enantiomer InChIKey | ICSUAADVGLPLFO-UMCMBGNQSA-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-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[6-[(TOL-4-YL)-SULFONYLOXY]-HEXYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[4-[(TOL-4-YL)-SULFONYLOXY]-BUTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[3-[(TOL-4-YL)-SULFONYLOXY]-PROPYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[5-(TETRAHYDRO-2H-PYRAN-2-YL)-PENTYL]-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-[4-(TETRAHYDRO-2H-PYRAN-2-YL)-BUTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE
5'-Acetyl-2',3'-isopropylideneadenosine
| 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 |