L-2'-deoxycytidine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C9H13N3O4
- PM
- 227.22
- Pureté
- >=97%
L-2'-deoxycytidine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxycytidine. CH64042 is identified by CAS 40093-94-5, molecular formula C9H13N3O4, molecular weight 227.22, and PubChem CID 159354.
The cited mirror-image oligonucleotide literature discusses L-configured nucleotides as systems with high biostability in nuclease-related studies. CH64042 provides the L-2'-deoxycytidine identity for related L-DNA, aptamer, and nucleoside stereochemistry research.
Synonymes
L-2'-deoxycytidine; β-L-2'-deoxycytidine; L-dC
Identité et spécifications
| Catalog No. | CH64042 |
| CAS No. | 40093-94-5 |
| Molecular Formula | C9H13N3O4 |
| Molecular Weight | 227.22 |
| PubChem CID | 159354 |
| InChIKey | CKTSBUTUHBMZGZ-CHKWXVPMSA-N |
| Purity | >=97% |
Conditions de stockage
2-8 C
Caractéristiques techniques
- Nucleobase
- Cytosine
- Sugar
- L-2'-Deoxyribose
- Nucleoside class
- Pyrimidine L-deoxyribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- 1 mL solution; 2 mg powder; Custom packaging on request
- Solution concentration
- 10 mM in DMSO
- Physical form
- White to off-white powder
- Stability
- 3 years as powder; 1 year in solvent
Contexte d’application
- Mirror-image L-DNA research: CH64042 is relevant to studies of mirror-image L-DNA oligonucleotides and aptamer systems.
- Enantiomeric deoxynucleoside studies: L-2'-deoxycytidine provides the deoxycytidine mirror-image identity for stereochemistry and biostability comparisons.
- L-deoxynucleoside reference: CH64042 provides the L-2'-deoxycytidine 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 159354
PubChem · CID 159354
Questions fréquentes
How is L-2'-deoxycytidine different from 2'-deoxycytidine?
L-2'-deoxycytidine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxycytidine. They share molecular formula and mass but have opposite chirality; the natural form is cataloged separately.
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