CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-5-Methyluridine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

製品番号CH64040CAS番号642082-80-2純度>=98%
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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
C10H14N2O6
分子量
258.23
純度
>=98%

L-5-Methyluridine, also called L-ribothymidine, is the L-enantiomer, or mirror-image form, of natural D-5-methyluridine. CH64040 is identified by CAS 642082-80-2, molecular formula C10H14N2O6, molecular weight 258.23, and PubChem CID 1715220.

The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64040 provides the L-5-methyluridine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.

別名

L-5-Methyluridine; L-ribothymidine; β-L-5-methyluridine

同定情報と仕様

Catalog No.CH64040
CAS No.642082-80-2
Molecular FormulaC10H14N2O6
Molecular Weight258.23
PubChem CID1715220
InChIKeyDWRXFEITVBNRMK-AZRUVXNYSA-N
Purity>=98%

保管条件

2-8 C

技術属性

Nucleobase
5-Methyluracil
Sugar
L-Ribose
Nucleoside class
Modified pyrimidine L-ribonucleoside
Research role
Mirror-image nucleic-acid building-block reference
Packaging
Custom packaging on request
Physical form
White to off-white powder

用途情報

  • Mirror-image / Spiegelmer research: CH64040 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
  • Enantiomeric nucleoside studies: L-5-methyluridine provides the 5-methyluridine mirror-image identity for stereochemistry and biostability comparisons.
  • L-nucleoside reference: CH64040 provides the L-5-methyluridine identity for nucleoside chemistry research.

関連技術資料

公開情報源

よくある質問

How is L-5-methyluridine different from 5-methyluridine?

L-5-Methyluridine (L-ribothymidine) is the L-enantiomer, or mirror-image form, of natural D-5-methyluridine. They share molecular formula and mass but have opposite chirality; the natural form is cataloged separately.

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