CAS 707-99-3: 9-(2-Hydroxyethyl)adenine
Formula:C7H9N5O
InChI:InChI=1S/C7H9N5O/c8-6-5-7(10-3-9-6)12(1-2-13)4-11-5/h3-4,13H,1-2H2,(H2,8,9,10)
InChI key:InChIKey=VAQOTZQDXZDBJK-UHFFFAOYSA-N
SMILES:C(CO)N1C=2C(=C(N)N=CN2)N=C1
Synonyms:- 2-(6-Amino-9H-purin-9-yl)ethan-1-ol
- 2-(6-amino-9H-purin-9-yl)ethanol
- 6-Amino-9H-Purin-9-Ethanol
- 6-Amino-9H-purine-9-ethanol
- 9-(2-Hydroxyethyl) Adenine
- 9-(β-Hydroxyethyl)adenine
- 9H-Purine-9-ethanol, 6-amino-
- NSC 51467
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Found 7 products.
2-(6-Aminopurin-9-yl)ethanol
CAS:Controlled ProductApplications 2-(6-Aminopurin-9-yl)ethanol is a useful intermediate in the preparation of aryloxyalkyl derivatives of adenine with antiviral activity. References Petrov, V. I., et al.: Chemistry of Heterocyclic Compounds, 39, 1218 (2003)Formula:C7H9N5OColor and Shape:NeatMolecular weight:179.189-(2-Hydroxyethyl)adenine
CAS:9-(2-Hydroxyethyl)adenine is a synthetic adenine derivative that has been used in the study of the structural and functional theory of DNA. It is a residue that is found in both RNA and DNA. Adenine forms hydrogen bonds with thymine, guanine, cytosine and uracil. 9-(2-Hydroxyethyl)adenine can be used to analyze environmental pollution by measuring the amount of free hydroxyl radicals present in a sample. It reacts spontaneously with other molecules at constant rates, but its reaction time depends on the number of complex molecules it interacts with. 9-(2-Hydroxyethyl)adenine has been shown to have anticancer effects on carcinoma cells by inhibiting ribonucleotide reductase activity.Formula:C7H9N5OPurity:Min. 95%Molecular weight:179.18 g/mol2-(6-Aminopurin-9-yl)ethanol
CAS:Formula:C7H9N5OPurity:98%Color and Shape:SolidMolecular weight:179.17939-(2-Hydroxyethyl)adenine
CAS:Formula:C7H9N5OPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:179.182-(6-Aminopurin-9-yl)ethanol
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:179.18299865722656
