N6-Anisoyladenosine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- MF
- C18H19N5O6
- MW
- 401.4
- Purity
- >=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.
Synonyms
N6-Anisoyladenosine; N6-(4-methoxybenzoyl)adenosine; N6-PAc-rA; PAc-rA
Identity and specifications
| Catalog No. | CH64080 |
| CAS No. | 56883-05-7 |
| Molecular Formula | C18H19N5O6 |
| Molecular Weight | 401.4 |
| PubChem CID | 10092434 |
| InChIKey | YDVLBCYELIMFHS-XWXWGSFUSA-N |
| Purity | >=98% |
Technical attributes
- 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
Application context
- 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.
Related technical resources
Oligonucleotide Modification
Sugar, base, backbone, terminal, and conjugation modifications for ASO, siRNA, guide RNA, aptamer, and research or labeling oligo projects.
Oligonucleotide Synthesis
Support for modified monomers, supports, sulfurizing reagents, cap analogs, and related oligo synthesis inputs.
Public references
- 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
- PubChem Compound 10092434
PubChem · CID 10092434
Frequently Asked Questions
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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