Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-rA (Bz) CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

제품 번호CH65086CAS 번호1803193-36-3순도>=98.0% (HPLC)
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제품 개요

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제품군
Oligonucleotide Synthesis, RNA Raw Materials & Modification
분자식
C53H66N7O8PSi
분자량
988.2
순도
>=98.0% (HPLC)

L-rA (Bz) CE Phosphoramidite is a mirror-image RNA building block: 5'-O-(4,4'-dimethoxytrityl)-N6-benzoyl-2'-O-(tert-butyldimethylsilyl)-L-adenosine 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite. It is identified by CAS 1803193-36-3, molecular formula C53H66N7O8PSi, molecular weight 988.2, PubChem CID 13872239, and InChIKey FFXHNCNNHASXCT-XMSTWNTJSA-N.

It is the enantiomer of the natural D-adenosine 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 N6-benzoyl base-protecting group is removed during final deprotection.

동의어

5'-O-DMT-N6-Bz-2'-O-TBDMS-L-adenosine 3'-CE phosphoramidite; L-riboadenosine (mirror-image) amidite

식별 정보 및 규격

Catalog No.CH65086
CAS No.1803193-36-3
Molecular FormulaC53H66N7O8PSi
Molecular Weight988.2
PubChem CID13872239
InChIKeyFFXHNCNNHASXCT-XMSTWNTJSA-N
Purity>=98.0% (HPLC)

보관 조건

2 to 8 C

기술 속성

Monomer class
2'-O-TBDMS L-RNA CE phosphoramidite
Nucleobase
Adenine
Sugar configuration
L-ribose
Base protection
N6-benzoyl
Packaging
100 mg; 250 mg; 1 g; Custom packaging on request
Physical form
white to off-white powder

응용 맥락

  • Mirror-image (L-ribose) monomer: provides the L-adenosine 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 N6-benzoyl base-protecting group is removed during final deprotection.

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