2',3',5'-Tri-O-acetyl-D-adenosine
[(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methyl acetate
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Nom chimique
- [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methyl acetate
- FM
- C16H19N5O7
- PM
- 393.35
- Pureté
- >=97%
2',3',5'-Tri-O-acetyl-D-adenosine is a protected adenosine derivative for nucleoside chemistry and adenosine-derivative synthesis research. It is also referenced as 2',3',5'-Tri-O-acetyladenosine, Tri-O-acetyladenosine, and adenosine 2',3',5'-triacetate.
CH58005 is listed with CAS 7387-57-7, molecular formula C16H19N5O7, and molecular weight 393.35. The compound fits literature and project records that involve protected adenosine derivatives, N6-substituted adenosine synthesis, or regioselective adenosine-derivative modification.
Synonymes
2',3',5'-Tri-O-acetyladenosine; Adenosine, 2',3',5'-triacetate; Tri-O-acetyladenosine; Adenosine 2',3',5'-triacetate
Identité et spécifications
| Catalog No. | CH58005 |
| CAS No. | 7387-57-7 |
| Molecular Formula | C16H19N5O7 |
| Molecular Weight | 393.35 |
| PubChem CID | 96503 |
| InChIKey | GCVZNVTXNUTBFB-XNIJJKJLSA-N |
| Purity | >=97% |
Conditions de stockage
-20 C; protect from light
Caractéristiques techniques
- Nucleoside scaffold
- Adenosine
- Sugar protection
- 2',3',5'-tri-O-acetyl
- Material role
- Protected nucleoside derivative
- Packaging
- Custom packaging on request
- Physical form
- White to off-white powder
Contexte d’application
- Protected nucleoside synthesis: relevant to synthesis research built around protected adenosine and nucleoside derivatives.
- Adenosine-derivative modification: reported in workflows involving N6-substituted adenosines and regioselective modification of adenosine derivatives.
- Name reconciliation: helps match records that use Tri-O-acetyladenosine or adenosine 2',3',5'-triacetate naming.
Ressources techniques associées
Sources publiques
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- Composé PubChem 96503
PubChem · CID 96503
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