Oligonucleotide Synthesis, RNA Raw Materials & Modification

2'-OMe-Guanosine (dmf) CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

Produkt-Nr.CH65021CAS-Nr.128219-77-2Reinheit>=98.5% (HPLC)
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Produktübersicht

Kurzüberblick

Produktfamilie
Oligonucleotide Synthesis, RNA Raw Materials & Modification
MF
C44H55N8O8P
MW
854.9
Reinheit
>=98.5% (HPLC)

2'-OMe-Guanosine (dmf) CE Phosphoramidite is the 2'-O-methyl guanosine building block for modified-RNA synthesis: 5'-O-(4,4'-dimethoxytrityl)-N2-dimethylformamidine-2'-O-methylguanosine bearing a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite group. CH65021 is identified by CAS 128219-77-2, molecular formula C44H55N8O8P, molecular weight 854.9, PubChem CID 135742510, and InChIKey ZGDBCILCTOHNAB-OWKWDSSOSA-N.

Nucleoside phosphoramidites are the coupling monomers used in automated solid-phase oligonucleotide synthesis: the 3'-phosphoramidite couples to the growing chain, the acid-labile 5'-DMT is removed each cycle, and the N2-dmf base group is removed at final deprotection. In the cited literature, 2'-O-methyl ribonucleosides/residues are discussed for nuclease resistance and RNA affinity.

Synonyme

DMT-2'-OMe-rG(dmf) phosphoramidite; 5'-O-DMT-N2-dmf-2'-O-methylguanosine 3'-CE phosphoramidite

Identität und Spezifikationen

Catalog No.CH65021
CAS No.128219-77-2
Molecular FormulaC44H55N8O8P
Molecular Weight854.9
PubChem CID135742510
InChIKeyZGDBCILCTOHNAB-OWKWDSSOSA-N
Purity>=98.5% (HPLC)

Lagerbedingungen

-20 C

Technische Merkmale

Monomer class
2'-O-methyl RNA CE phosphoramidite
Nucleobase
Guanine
Sugar modification
2'-O-Methyl
Base protection
N2-Dimethylaminomethylene (dmf)
Grade
N (Normal)
Packaging
100 mg; 250 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 100 g; 200 g; Custom packaging on request
Water content
<=0.5%
Physical form
white to off-white powder
Stability
>=4 years

Anwendungskontext

  • 2'-OMe RNA coupling monomer: the 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite is the reactive group that couples to the growing oligonucleotide chain in automated solid-phase synthesis.
  • 2'-OMe sugar modification: cited 2'-O-methyl oligonucleotide literature discusses nuclease resistance and RNA affinity.
  • 5'-DMT + N2-dmf protection: the acid-labile 5'-DMT is removed each cycle, and the N2-dimethylformamidine base group is removed at final deprotection.

Zugehörige technische Ressourcen

Öffentliche Quellen

Häufig gestellte Fragen

What does this 2'-OMe amidite do in RNA synthesis?

Its 3'-phosphoramidite couples to the growing chain, with 5'-DMT removed each cycle and N2-dmf removed at final deprotection. The product provides a 2'-O-methylguanosine phosphoramidite identity.

How does it differ from the 2'-OMe-G(iBu) phosphoramidite?

Both are 2'-O-methyl guanosine amidites, but this one uses an N2-dimethylformamidine (dmf) base protection rather than isobutyryl. The isobutyryl amidite is cataloged separately.

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