Oligonucleotide Synthesis, RNA Raw Materials & Modification

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

Oligonucleotide Synthesis, RNA Raw Materials & Modification

製品番号CH65012CAS番号147201-04-5純度100.0% (NMR)

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製品概要

クイックビュー

製品ファミリー: Oligonucleotide Synthesis, RNA Raw Materials & Modification
分子式: C50H68N7O9PSi
分子量: 970.2
純度: 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.

別名

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

同定情報と仕様

Catalog No.	CH65012
CAS No.	147201-04-5
Molecular Formula	C50H68N7O9PSi
Molecular Weight	970.2
PubChem CID	135587729
InChIKey	PGJKESPHANLWME-FTZVBZPOSA-N
Purity	100.0% (NMR)

保管条件

-20 C; dry, inert atmosphere

技術属性

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

用途情報

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.

公開情報源

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化合物 135587729
PubChem · CID 135587729

よくある質問

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.