2,2'-O-Anhydro-5-methyluridine

98.0%

  • Product Code: 126930
  Alias:    2,2'-O-anhydro-5-methyluridine 2,2'-Anhydro-(1-β-D-arabinofuranosyl)-5-methyluracil
  CAS:    22423-26-3
Molecular Weight: 240.22 g./mol Molecular Formula: C₁₀H₁₂N₂O₅
EC Number: MDL Number: MFCD00233555
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: Used primarily in the synthesis of modified nucleosides, it plays a crucial role in the development of antiviral and anticancer drugs. This compound is a key intermediate in the production of nucleoside analogs, which are designed to inhibit the replication of viruses and cancer cells by interfering with their nucleic acid synthesis. It is also utilized in research to study the mechanisms of RNA and DNA synthesis, aiding in the understanding of genetic processes and the development of targeted therapies. Additionally, it finds applications in the field of biochemistry for the modification of nucleic acids, enabling the exploration of their structure and function.
Product Specification:
Test Specification
Appearance White To Off-White To Very Pale Yellow To Yellow Powder Or Crystals
Purity (%) 97.5-100
Specific Rotation [α]24/D(C=4, H2O) -46.0 to -43.0
Melting Point 217.0-226.0
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €10.29
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5.000 10-20 days €19.00
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25.000 10-20 days €36.93
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100.000 10-20 days €120.04
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2,2'-O-Anhydro-5-methyluridine
Used primarily in the synthesis of modified nucleosides, it plays a crucial role in the development of antiviral and anticancer drugs. This compound is a key intermediate in the production of nucleoside analogs, which are designed to inhibit the replication of viruses and cancer cells by interfering with their nucleic acid synthesis. It is also utilized in research to study the mechanisms of RNA and DNA synthesis, aiding in the understanding of genetic processes and the development of targeted therapies. Additionally, it finds applications in the field of biochemistry for the modification of nucleic acids, enabling the exploration of their structure and function.
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