Oligonucleotide Synthesis, RNA Raw Materials & Modification

2'-O-MOE-5-Methyluridine CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

产品编号CH65036CAS号163878-63-5纯度100% (HPLC)
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产品概述

快速信息

产品系列
Oligonucleotide Synthesis, RNA Raw Materials & Modification
分子式
C43H55N4O10P
分子量
818.9
纯度
100% (HPLC)

2'-O-MOE-5-Methyluridine CE Phosphoramidite is the 2'-O-methoxyethyl 5-methyluridine building block for modified-RNA synthesis: 5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine (5-methyluracil base) bearing a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite group. CH65036 is identified by CAS 163878-63-5, molecular formula C43H55N4O10P, molecular weight 818.9, PubChem CID 92043625, and InChIKey YFRRKZDUDXHJNC-KZQAAKLLSA-N.

Nucleoside phosphoramidites are the coupling monomers used in automated solid-phase oligonucleotide synthesis: the 3'-phosphoramidite couples to the growing chain and the acid-labile 5'-DMT is removed each cycle. Because the 5-methyluracil base has no exocyclic amine, no base protecting group is required. In the cited structure and stability literature, 2'-O-MOE ribonucleosides/residues are discussed in RNA-affinity and nuclease-resistance studies and as flanking residues in gapmer antisense oligonucleotides.

同义词

DMT-2'-O-MOE-5Me-rU phosphoramidite; 5'-O-DMT-2'-O-MOE-5-methyluridine 3'-CE phosphoramidite

身份与规格

Catalog No.CH65036
CAS No.163878-63-5
Molecular FormulaC43H55N4O10P
Molecular Weight818.9
PubChem CID92043625
InChIKeyYFRRKZDUDXHJNC-KZQAAKLLSA-N
Purity100% (HPLC)

储存条件

-20 C

技术属性

Monomer class
2'-O-MOE RNA CE phosphoramidite
Nucleobase
5-Methyluracil
Sugar modification
2'-O-(2-Methoxyethyl) (MOE)
Base protection
Unprotected
Grade
N (Normal)
Packaging
250 mg; 500 mg; 1 g; 2 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
lot expiration 5 September 2026

应用背景

  • 2'-MOE 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'-MOE sugar modification: cited structure and stability literature discusses 2'-O-MOE residues in RNA-affinity and nuclease-resistance studies and as gapmer flank residues.
  • No base protection needed: the 5-methyluracil base has no exocyclic amine, so this monomer requires no base protecting group (only the acid-labile 5'-DMT, removed each cycle).

相关技术资源

公开来源

常见问题

Why does this 2'-MOE amidite have no base protecting group?

Its base is 5-methyluracil, which has no reactive exocyclic amine, so it needs no base protection. The monomer carries the acid-labile 5'-O-DMT group, removed each cycle, and the 3'-phosphoramidite coupling group.

How does it relate to 5'-O-DMT-2'-O-MOE-5-methyluridine?

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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