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2'-Deoxyadenosine monohydrate, 99%
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Catalog number A11166.03
also known as A11166-03
Price (USD)/ Each
35.65
Online exclusive
39.00 Save 3.35 (9%)
-
Quantity:
1 g
Price (USD)/ Each
35.65
Online exclusive
39.00 Save 3.35 (9%)
2'-Deoxyadenosine monohydrate, 99%
Catalog numberA11166.03
Price (USD)/ Each
35.65
Online exclusive
39.00 Save 3.35 (9%)
-
Chemical Identifiers
CAS16373-93-6
IUPAC Name(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol
Molecular FormulaC10H13N5O3
InChI KeyOLXZPDWKRNYJJZ-YUZWJPFSNA-N
SMILESNC1=C2N=CN([C@H]3C[C@H](O)[C@@H](CO)O3)C2=NC=N1
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Specifications
Specification Sheet
Specification SheetWater Content (Karl Fischer Titration)5.0 to 8.0% (theory 6.69%)
Optical Rotation-25.3? ± 1.5? (c = 0.5, Water)
Appearance (Color)White
Assay (HPLC)≥98.5%
Melting Point (clear melt)188.0-194.0?C
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2?-Deoxyadenosineise is used by some cells as an energy source under energy stress conditions and to affect cAMP levels. 2?-dAdo is used in comparison studies of the functions of adenosine analogues on various biological processes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2′-Deoxyadenosineise is used by some cells as an energy source under energy stress conditions and to affect cAMP levels. 2′-dAdo is used in comparison studies of the functions of adenosine analogues on various biological processes.
Solubility
Soluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
2′-Deoxyadenosineise is used by some cells as an energy source under energy stress conditions and to affect cAMP levels. 2′-dAdo is used in comparison studies of the functions of adenosine analogues on various biological processes.
Solubility
Soluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Ashley M. Berman.; Jeffrey S. Johnson. Copper-Catalyzed Electrophilic Amination of Organozinc Nucleophiles: Documentation of O-Benzoyl Hydroxylamines as Broadly Useful R2N(+) and RHN(+) Synthons. J. Org. Chem. 2006, 71, (1), 219-224.
- Songbai Liu, Lanny S. Liebeskind. A Simple, Modular Synthesis of Substituted Pyridines. J. Am. Chem. Soc. 2008, 130, (22), 6918-6919.