L-5-Methyluridine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Resumen del producto
Vista rápida
- Familia de productos
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C10H14N2O6
- PM
- 258.23
- Pureza
- >=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.
Sinónimos
L-5-Methyluridine; L-ribothymidine; β-L-5-methyluridine
Identidad y especificaciones
| Catalog No. | CH64040 |
| CAS No. | 642082-80-2 |
| Molecular Formula | C10H14N2O6 |
| Molecular Weight | 258.23 |
| PubChem CID | 1715220 |
| InChIKey | DWRXFEITVBNRMK-AZRUVXNYSA-N |
| Purity | >=98% |
Condiciones de almacenamiento
2-8 C
Atributos técnicos
- 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
Contexto de aplicación
- 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.
Recursos técnicos relacionados
Fuentes públicas
- 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
- Compuesto de PubChem 1715220
PubChem · CID 1715220
Preguntas frecuentes
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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