L-rC (Ac) CE Phosphoramidite
Oligonucleotide Synthesis, RNA Raw Materials & Modification
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
- C47H64N5O9PSi
- 分子量
- 902.1
- 純度
- >=98%
L-rC (Ac) CE Phosphoramidite is a mirror-image RNA building block: 5'-O-(4,4'-dimethoxytrityl)-N4-acetyl-2'-O-(tert-butyldimethylsilyl)-L-cytidine 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite. It is identified by CAS 237060-94-5, molecular formula C47H64N5O9PSi, molecular weight 902.1, PubChem CID 70700204, and InChIKey QKWKXYVKGFKODW-ZYRNLWDWSA-N.
It is the enantiomer of the natural D-cytidine amidite — built on L-ribose rather than D-ribose — so it has the same molecular formula and weight as its D-counterpart. The cited mirror-image oligonucleotide literature provides background for L-configured oligonucleotide chemistry and D/L strand-pairing orthogonality. The 2'-O-TBDMS group protects the 2'-hydroxyl, the 5'-DMT is removed each cycle, and the N4-acetyl base-protecting group is removed during final deprotection.
別名
5'-O-DMT-N4-Ac-2'-O-TBDMS-L-cytidine 3'-CE phosphoramidite; L-ribocytidine (mirror-image) amidite
同定情報と仕様
| Catalog No. | CH65087 |
| CAS No. | 237060-94-5 |
| Molecular Formula | C47H64N5O9PSi |
| Molecular Weight | 902.1 |
| PubChem CID | 70700204 |
| InChIKey | QKWKXYVKGFKODW-ZYRNLWDWSA-N |
| Purity | >=98% |
保管条件
2 to 8 C
技術属性
- Monomer class
- 2'-O-TBDMS L-RNA CE phosphoramidite
- Nucleobase
- Cytosine
- Sugar configuration
- L-ribose
- Base protection
- N4-acetyl
- Grade
- N (Normal)
- Packaging
- 100 mg; 250 mg; 1 g; 5 g; 10 g; 25 g; Custom packaging on request
- Physical form
- white to off-white powder
用途情報
- Mirror-image (L-ribose) monomer: provides the L-cytidine subunit identity for L-RNA synthesis.
- Mirror-image literature context: cited literature supports L-configured oligonucleotide chemistry and D/L strand-pairing orthogonality.
- RNA protection scheme: 2'-O-TBDMS protects the 2'-hydroxyl, the 5'-DMT is removed each cycle, and the N4-acetyl base-protecting group is removed during final deprotection.
関連技術資料
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 70700204
PubChem · CID 70700204
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