N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-5'-O-[6-(TETRAHYDRO-2H-PYRAN-2-YL)-HEXYL]-ADENOSINE
Compound with spectra: 1 NMR
![N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-5'-O-[6-(TETRAHYDRO-2H-PYRAN-2-YL)-HEXYL]-ADENOSINE](/api/compound/2pZ5XZvrIjc.png?ph=true&h=300&w=458 "N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-5'-O-[6-(TETRAHYDRO-2H-PYRAN-2-YL)-HEXYL]-ADENOSINE")
| SpectraBase Compound ID | 2pZ5XZvrIjc |
|---|---|
| InChI | InChI=1S/C31H41N5O7/c1-31(2)42-25-22(18-38-15-9-3-4-10-16-39-23-14-8-11-17-40-23)41-30(26(25)43-31)36-20-34-24-27(32-19-33-28(24)36)35-29(37)21-12-6-5-7-13-21/h5-7,12-13,19-20,22-23,25-26,30H,3-4,8-11,14-18H2,1-2H3,(H,32,33,35,37)/t22-,23?,25-,26-,30-/m0/s1 |
| InChIKey | KFJDIEFQBWGLQG-LJJJVMCRSA-N |
| Mol Weight | 595.7 g/mol |
| Molecular Formula | C31H41N5O7 |
| Exact Mass | 595.300599 g/mol |
| Enantiomer InChIKey | KFJDIEFQBWGLQG-MQRNIKAISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-5'-O-[4-(TETRAHYDRO-2H-PYRAN-2-YL)-BUTYL]-ADENOSINE
N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-5'-O-[3-(TETRAHYDRO-2H-PYRAN-2-YL)-PROPYL]-ADENOSINE
N6-BENZOYL-2',3'-O-ISOPROPYLIDENE-ADENOSINE
MOJXTABXVXMEQH-KSTYGINMSA-N
N-[9-[(3aR,4R,6R,6aR)-2,2-dimethyl-4-methylol-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]purin-6-yl]carbamic acid benzyl ester
6-N-Benzoyl-9-(5,6-dideoxy-2,3-O-isopropylidene-.beta.-D-ribo-hex-5-enofuranosyl)adenine
6-N-Benzoyl-9-[6-(E/Z)-(tributylstannyl)-5,6-dideoxy-2,3-O-isopropylidene-.beta.,D-ribo-hex-5-enfuranosyl]adenine
2',3'-ISOPROPYLIDENE-N6-AMINOETHYL-ADENOSINE-5'-MONOPHOSPHATE;N6-AE-AMP-AC
2',3'-ISOPROPYLIDENE-N6-[((DIOCTADECYL)-AMINO)-SUCCINYL-AMINOHEXYL]-ADENOSINE-5'-MONOPHOSPHATE;DODA-HM-N6-AMP-AC
2',3'-ISOPROPYLIDENE-N6-AMINOHEXYL-ADENOSINE-5'-MONOPHOSPHATE;N6-HM-AMP-AC
| 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 |