Oligonucleotide Synthesis, RNA Raw Materials & Modification

N6-Anisoyladenosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

Product NoCH64080CAS No56883-05-7Purity>=98%
N6-Anisoyladenosine

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 FormulaC18H19N5O6
Molecular Weight401.4
PubChem CID10092434
InChIKeyYDVLBCYELIMFHS-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.

Public references

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.

What identifiers should match for CH64080?

Use CAS 56883-05-7, molecular formula C18H19N5O6, molecular weight 401.4, PubChem CID 10092434, and InChIKey YDVLBCYELIMFHS-XWXWGSFUSA-N.

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