CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-2'-deoxyuridine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

N.º de productoCH64044N.º CAS31501-19-6Pureza>=97%
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Resumen del producto

Vista rápida

Familia de productos
Oligonucleotide Synthesis, RNA Raw Materials & Modification
FM
C9H12N2O5
PM
228.20
Pureza
>=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.

Sinónimos

L-2'-deoxyuridine; β-L-2'-deoxyuridine; L-dU

Identidad y especificaciones

Catalog No.CH64044
CAS No.31501-19-6
Molecular FormulaC9H12N2O5
Molecular Weight228.20
PubChem CID453556
InChIKeyMXHRCPNRJAMMIM-GKROBHDKSA-N
Purity>=97%

Condiciones de almacenamiento

2-8 C

Atributos técnicos

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

Contexto de aplicación

  • 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.

Recursos técnicos relacionados

Fuentes públicas

Preguntas frecuentes

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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