Oligonucleotide Synthesis, RNA Raw Materials & Modification

2'-O-TBDMS-Guanosine (iBu) CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

Produkt-Nr.CH65012CAS-Nr.147201-04-5Reinheit100.0% (NMR)
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Produktübersicht

Kurzüberblick

Produktfamilie
Oligonucleotide Synthesis, RNA Raw Materials & Modification
MF
C50H68N7O9PSi
MW
970.2
Reinheit
100.0% (NMR)

2'-O-TBDMS-Guanosine (iBu) CE Phosphoramidite is the fully protected guanosine building block for RNA synthesis: 5'-O-(4,4'-dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)-N2-isobutyrylguanosine bearing a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite group. CH65012 is identified by CAS 147201-04-5, molecular formula C50H68N7O9PSi, molecular weight 970.2, PubChem CID 135587729, and InChIKey PGJKESPHANLWME-FTZVBZPOSA-N.

Nucleoside phosphoramidites are the coupling monomers used in automated solid-phase RNA synthesis: the 3'-phosphoramidite is the reactive group that couples to the growing chain, the acid-labile 5'-DMT is removed at the start of each cycle, the 2'-O-TBDMS protects the ribose 2'-hydroxyl, and the N2-isobutyryl base group is removed at final deprotection.

Synonyme

DMT-2'-O-TBDMS-rG(iBu) phosphoramidite; 5'-O-DMT-2'-O-TBDMS-N2-isobutyrylguanosine 3'-CE phosphoramidite

Identität und Spezifikationen

Catalog No.CH65012
CAS No.147201-04-5
Molecular FormulaC50H68N7O9PSi
Molecular Weight970.2
PubChem CID135587729
InChIKeyPGJKESPHANLWME-FTZVBZPOSA-N
Purity100.0% (NMR)

Lagerbedingungen

-20 C; dry, inert atmosphere

Technische Merkmale

Monomer class
RNA CE phosphoramidite
Nucleobase
Guanine
2'-O protection
TBDMS (tert-butyldimethylsilyl)
Base protection
N2-Isobutyryl
Grade
N (Normal)
Packaging
250 mg; 500 mg; 1 g; 2 g; 5 g; 10 g; 25 g; 50 g; 100 g; 200 g; Custom packaging on request
Water content
<=0.3%
Physical form
white to faint yellow powder
Stability
Manufactured 2023-05-30; retest 2026-11-30; expiry 2027-05-29

Anwendungskontext

  • 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 RNA synthesis.
  • 5'-DMT + 2'-O-TBDMS protection: the acid-labile 5'-DMT is removed each cycle, while the 2'-O-TBDMS group protects the ribose 2'-hydroxyl during synthesis.
  • N2-isobutyryl base protection: the isobutyryl group masks the guanine exocyclic amine during synthesis and is removed at final deprotection.

Zugehörige technische Ressourcen

Öffentliche Quellen

Häufig gestellte Fragen

What are the four functional groups on this RNA amidite?

A 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite (the reactive coupling group), an acid-labile 5'-O-DMT group (removed each cycle), a 2'-O-TBDMS group (protects the ribose 2'-hydroxyl), and an N2-isobutyryl base protection (removed at final deprotection).

How does it relate to 5'-O-DMT-2'-O-TBDMS-N2-isobutyrylguanosine?

It is the phosphoramidite of that nucleoside: the 3'-hydroxyl has been converted to a 2-cyanoethyl N,N-diisopropyl phosphoramidite. The precursor is cataloged separately.

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