5'-O-Acetyl-2',3'-O-isopropylideneadenosine
95%
- Product Code: 36067
CAS:
15888-38-7
Molecular Weight: | 349.3419 g./mol | Molecular Formula: | C₁₅H₁₉N₅O₅ |
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EC Number: | MDL Number: | MFCD00005755 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
5'-O-Acetyl-2',3'-O-isopropylideneadenosine is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a protected form of adenosine, which is crucial for the development of nucleoside analogs. These analogs are often explored for their potential therapeutic applications, particularly in antiviral and anticancer drug development. The protective groups (acetyl and isopropylidene) allow for selective modification of the adenosine molecule, enabling researchers to synthesize specific derivatives with desired biological activities. This compound is also valuable in studying enzyme mechanisms and nucleotide interactions, as it provides a stable intermediate for further chemical transformations. Its application extends to the synthesis of modified RNA and DNA sequences, which are essential in molecular biology and genetic engineering research.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,818.00 |
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5'-O-Acetyl-2',3'-O-isopropylideneadenosine
5'-O-Acetyl-2',3'-O-isopropylideneadenosine is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a protected form of adenosine, which is crucial for the development of nucleoside analogs. These analogs are often explored for their potential therapeutic applications, particularly in antiviral and anticancer drug development. The protective groups (acetyl and isopropylidene) allow for selective modification of the adenosine molecule, enabling researchers to synthesize specific derivatives with desired biological activities. This compound is also valuable in studying enzyme mechanisms and nucleotide interactions, as it provides a stable intermediate for further chemical transformations. Its application extends to the synthesis of modified RNA and DNA sequences, which are essential in molecular biology and genetic engineering research.
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