L-Adenosine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Resumen del producto
Vista rápida
- Familia de productos
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C10H13N5O4
- PM
- 267.24
- Pureza
- >=95.0%
L-Adenosine is the L-enantiomer, or mirror-image form, of natural D-adenosine. CH64035 is identified by CAS 3080-29-3, molecular formula C10H13N5O4, molecular weight 267.24, and PubChem CID 448374.
The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64035 provides the L-adenosine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.
Sinónimos
L-Adenosine; β-L-adenosine
Identidad y especificaciones
| Catalog No. | CH64035 |
| CAS No. | 3080-29-3 |
| Molecular Formula | C10H13N5O4 |
| Molecular Weight | 267.24 |
| PubChem CID | 448374 |
| InChIKey | OIRDTQYFTABQOQ-DEGSGYPDSA-N |
| Purity | >=95.0% |
Condiciones de almacenamiento
-20 C
Atributos técnicos
- Nucleobase
- Adenine
- Sugar
- L-Ribose
- Nucleoside class
- Purine L-ribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- 100 mg; 250 mg; 500 mg; 1 g; Custom packaging on request
- Water content
- <=0.5% loss on drying
- Physical form
- White to off-white crystalline powder
Contexto de aplicación
- Mirror-image / Spiegelmer research: CH64035 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
- Enantiomeric nucleoside studies: L-adenosine provides the adenosine mirror-image identity for stereochemistry and biostability comparisons.
- L-nucleoside reference: CH64035 provides the L-adenosine 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 448374
PubChem · CID 448374
Preguntas frecuentes
How is L-adenosine different from adenosine?
L-Adenosine is the L-enantiomer, or mirror-image form, of natural D-adenosine. They share molecular formula and mass but have opposite chirality; natural adenosine is cataloged separately.
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