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| IUPAC Name: | [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 4-methylbenzenesulfonate |
| Description: | 5'-Tosyl Adenosine is a chemically modified adenosine nucleotide in which the 5'-hydroxyl group of adenosine is substituted with a tosyl (p-toluenesulfonyl) group. This modification makes it a useful intermediate in organic synthesis and nucleoside chemistry. The tosyl group acts as a leaving group, facilitating various chemical reactions, such as nucleophilic substitutions, that can introduce other functional groups at the 5' position of adenosine. 5'-Tosyl Adenosine is often utilized in the preparation of modified nucleotides for research in biochemistry and molecular biology. |
| Molecular Weight: | 421.43 |
| Molecular Formula: | C17H19N5O6S |
| Canonical SMILES: | CC1=CC=C(C=C1)S(=O)(=O)OCC2C(C(C(O2)N3C=NC4=C3N=CN=C4N)O)O |
| InChI: | InChI=1S/C17H19N5O6S/c1-9-2-4-10(5-3-9)29(25,26)27-6-11-13(23)14(24)17(28-11)22-8-21-12-15(18)19-7-20-16(12)22/h2-5,7-8,11,13-14,17,23-24H,6H2,1H3,(H2,18,19,20)/t11-,13-,14-,17-/m1/s1 |
| InChI Key: | CAXLRAROZXYOHH-LSCFUAHRSA-N |
| Boiling Point: | 760.1±70.0 °C at 760 mmHg |
| Melting Point: | 151 °C |
| Purity: | ≥95% |
| Density: | 1.8±0.1 g/cm3 |
| Solubility: | Soluble in DMSO (Slightly), Methanol (Slightly, Heated) |
| Appearance: | White to off-white solid |
| Storage: | Store at 2-8 °C (under dark) |
| LogP: | 1.40360 |
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