Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-rC (Ac) CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

제품 번호CH65087CAS 번호237060-94-5순도>=98%
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제품 개요

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제품군
Oligonucleotide Synthesis, RNA Raw Materials & Modification
분자식
C47H64N5O9PSi
분자량
902.1
순도
>=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.

동의어

5'-O-DMT-N4-Ac-2'-O-TBDMS-L-cytidine 3'-CE phosphoramidite; L-ribocytidine (mirror-image) amidite

식별 정보 및 규격

Catalog No.CH65087
CAS No.237060-94-5
Molecular FormulaC47H64N5O9PSi
Molecular Weight902.1
PubChem CID70700204
InChIKeyQKWKXYVKGFKODW-ZYRNLWDWSA-N
Purity>=98%

보관 조건

2 to 8 C

기술 속성

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

응용 맥락

  • 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.

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