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Chemical Structure| 168427-74-5 Chemical Structure| 168427-74-5
Chemical Structure| 168427-74-5

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2′-O-(2-Methoxyethyl)adenosine is a modified adenosine derivative used in nucleic acid synthesis. Its modification enhances the stability and hydrophilicity of oligonucleotides, improving drug delivery efficiency in gene therapy.

Synonyms: 2′-O-(2-Methoxyethyl)adenosine

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Product Details of 2′-O-(2-Methoxyethyl)adenosine

CAS No. :168427-74-5
Formula : C13H19N5O5
M.W : 325.32
SMILES Code : COCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=CN=C2N
Synonyms :
2′-O-(2-Methoxyethyl)adenosine
MDL No. :MFCD02682961
InChI Key :PUDXUJRJLRLJIU-QYVSTXNMSA-N
Pubchem ID :11393191

Safety of 2′-O-(2-Methoxyethyl)adenosine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2′-O-(2-Methoxyethyl)adenosine

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 168427-74-5 ]

[ 168427-74-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 14316-61-1 ]
  • [ 168427-74-5 ]
  • N-{9-[(2R,3R,4R,5R)-4-Hydroxy-5-hydroxymethyl-3-(2-methoxy-ethoxy)-tetrahydro-furan-2-yl]-9H-purin-6-yl}-2-phenoxy-acetamide [ No CAS ]
  • 2
  • [ 16427-44-4 ]
  • [ 58-61-7 ]
  • [ 303197-30-0 ]
  • [ 1062491-29-5 ]
  • [ 1062491-27-3 ]
  • [ 168427-74-5 ]
  • 3
  • [ 16427-44-4 ]
  • [ 58-61-7 ]
  • [ 303197-30-0 ]
  • [ 1062491-29-5 ]
  • [ 168427-74-5 ]
  • 4
  • [ 16427-44-4 ]
  • [ 58-61-7 ]
  • [ 168427-74-5 ]
YieldReaction ConditionsOperation in experiment
56% With 2-methoxy-ethanol; sodium hydroxide; In N,N-dimethyl-formamide; at 8 - 65℃;Large scale; 10kg of Adenosine was added to 130L of anhydrous DMF and stirred to dissolve, then 50L anhydrous ethylene glycol monomethyl ether was added controlling the temperature 8-15C , added 6.89Kg of <strong>[16427-44-4]2-methoxyethyl methanesulfonate</strong> and 2.99Kg solid sodium hydroxide, stirred reaction was incubated 60-65C , HPLC monitoring completion of the reaction to the main raw material, then concentrated under reduced pressure at 60 degrees to dryness to give a brown oil as 2'-O-(2-methoxyethyl) adenosine.
 

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