2',3'-O-Isopropylideneguanosine

98.0%

  • Product Code: 126537
  Alias:    2',3'-O-isopropylideneguanosine
  CAS:    362-76-5
Molecular Weight: 323.3 g./mol Molecular Formula: C₁₃H₁₇N₅O₅
EC Number: 206-651-9 MDL Number: MFCD00057081
Melting Point: 296 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 2',3'-O-Isopropylideneguanosine is primarily used in the field of organic synthesis and biochemical research. It serves as a protected form of guanosine, where the isopropylidene group shields the 2' and 3' hydroxyl positions, preventing unwanted reactions during complex synthetic processes. This protection is crucial in the synthesis of nucleosides, nucleotides, and oligonucleotides, where selective reactivity is required. Additionally, it is utilized in the development of modified RNA and DNA analogs, aiding in the study of nucleic acid structure, function, and interactions. Its application extends to the production of antiviral and anticancer agents, where modified nucleosides play a key role in therapeutic strategies.
Product Specification:
Test Specification
Purity (HPLC) 98
Purity (Nonaqueous Titration) 97.5-100
Specific Rotation [A]20/D(C=1, 0.1MOL/L NaOH) -68
Specific Rotation [A]20/D(C=1, 0.1MOL/L NaOH) -73
Wavelength (pH 7.0) 252 nm-254 nm
Appearance White To Off-White Powder
Proton NMR Spectrum 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 €28.76
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25.000 10-20 days €110.80
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2',3'-O-Isopropylideneguanosine
2',3'-O-Isopropylideneguanosine is primarily used in the field of organic synthesis and biochemical research. It serves as a protected form of guanosine, where the isopropylidene group shields the 2' and 3' hydroxyl positions, preventing unwanted reactions during complex synthetic processes. This protection is crucial in the synthesis of nucleosides, nucleotides, and oligonucleotides, where selective reactivity is required. Additionally, it is utilized in the development of modified RNA and DNA analogs, aiding in the study of nucleic acid structure, function, and interactions. Its application extends to the production of antiviral and anticancer agents, where modified nucleosides play a key role in therapeutic strategies.
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