2'-Deoxyadenosine monohydrate, 99%
2'-Deoxyadenosine monohydrate, 99%
2'-Deoxyadenosine monohydrate, 99%
Thermo Scientific Chemicals

2'-Deoxyadenosine monohydrate, 99%

CAS: 16373-93-6 | C10H13N5O3 | 251.25 g/mol
Have Questions?
變更視圖buttonViewtableView
Quantity:
1 g
5 g
25 g
產品號碼 A11166.03
亦稱為 A11166-03
價格 (TWD)
-
Quantity:
1 g
Request bulk or custom format
化學識別
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
檢視更多
規格Specification Sheet規格表
Water 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
檢視更多
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.
RUO – Research Use Only

General References:

  1. 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.
  2. Songbai Liu, Lanny S. Liebeskind. A Simple, Modular Synthesis of Substituted Pyridines. J. Am. Chem. Soc. 2008, 130, (22), 6918-6919.