L-2'-deoxyuridine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C9H12N2O5
- PM
- 228.20
- Pureté
- >=97%
L-2'-deoxyuridine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxyuridine. CH64044 is identified by CAS 31501-19-6, molecular formula C9H12N2O5, molecular weight 228.20, and PubChem CID 453556.
The cited mirror-image oligonucleotide literature discusses L-configured nucleotides as systems with high biostability in nuclease-related studies. CH64044 provides the L-2'-deoxyuridine identity for related L-DNA, aptamer, and nucleoside stereochemistry research.
Synonymes
L-2'-deoxyuridine; β-L-2'-deoxyuridine; L-dU
Identité et spécifications
| Catalog No. | CH64044 |
| CAS No. | 31501-19-6 |
| Molecular Formula | C9H12N2O5 |
| Molecular Weight | 228.20 |
| PubChem CID | 453556 |
| InChIKey | MXHRCPNRJAMMIM-GKROBHDKSA-N |
| Purity | >=97% |
Conditions de stockage
2-8 C
Caractéristiques techniques
- Nucleobase
- Uracil
- Sugar
- L-2'-Deoxyribose
- Nucleoside class
- Pyrimidine L-deoxyribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- Custom packaging on request
- Physical form
- White to off-white powder
Contexte d’application
- Mirror-image L-DNA research: CH64044 is relevant to studies of mirror-image L-DNA oligonucleotides and aptamer systems.
- Enantiomeric deoxynucleoside studies: L-2'-deoxyuridine provides the deoxyuridine mirror-image identity for stereochemistry and biostability comparisons.
- L-deoxynucleoside reference: CH64044 provides the L-2'-deoxyuridine identity for nucleoside chemistry research.
Ressources techniques associées
Sources publiques
- 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
- Composé PubChem 453556
PubChem · CID 453556
Questions fréquentes
How is L-2'-deoxyuridine different from 2'-deoxyuridine?
L-2'-deoxyuridine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxyuridine. They share molecular formula and mass but have opposite chirality; the natural form is cataloged separately.
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