N6-Anisoyladenosine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C18H19N5O6
- PM
- 401.4
- Pureté
- >=98%
N6-Anisoyladenosine (N6-PAc-rA) is adenosine whose adenine exocyclic N6-amine is protected with a 4-methoxybenzoyl group. CH64080 is identified by CAS 56883-05-7, molecular formula C18H19N5O6, molecular weight 401.4, PubChem CID 10092434, and InChIKey YDVLBCYELIMFHS-XWXWGSFUSA-N.
The cited oligonucleotide-synthesis literature discusses exocyclic-amine protecting groups on nucleobases and their removal during deprotection. CH64080 provides the N6-(4-methoxybenzoyl)adenosine identity for RNA building-block and nucleoside chemistry research.
Synonymes
N6-Anisoyladenosine; N6-(4-methoxybenzoyl)adenosine; N6-PAc-rA; PAc-rA
Identité et spécifications
| Catalog No. | CH64080 |
| CAS No. | 56883-05-7 |
| Molecular Formula | C18H19N5O6 |
| Molecular Weight | 401.4 |
| PubChem CID | 10092434 |
| InChIKey | YDVLBCYELIMFHS-XWXWGSFUSA-N |
| Purity | >=98% |
Caractéristiques techniques
- Nucleobase
- Adenine
- Sugar
- D-Ribose
- Base protection
- N6-(4-Methoxybenzoyl) (anisoyl)
- Synthesis role
- Base-protected RNA nucleoside intermediate
- Packaging
- 10 mg; Custom packaging on request
Contexte d’application
- Base-protected RNA building block: the N6-(4-methoxybenzoyl) group masks the adenine exocyclic amine in RNA oligonucleotide-synthesis chemistry and is removed during deprotection.
- Adenosine (rA) monomer precursor context: CH64080 is the N6-(4-methoxybenzoyl)-protected adenosine identity relevant to adenine building-block preparation.
- Nucleoside chemistry reference: CH64080 provides the N6-anisoyladenosine identity for nucleoside chemistry research.
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 10092434
PubChem · CID 10092434
Questions fréquentes
What is the N6 protecting group on CH64080?
PubChem identifies CAS 56883-05-7 as N6-anisoyladenosine, with a 4-methoxybenzoyl group on the adenine exocyclic N6-amine.
How does it differ from N6-benzoyladenosine?
Both protect the adenine N6-amine, but CH64080 uses a 4-methoxybenzoyl group rather than benzoyl. N6-benzoyladenosine is cataloged separately.
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