2’,3’-O-Isopropylideneadenosine
98%
- Product Code: 126919
Alias:
2',3'-Isopropyladenosine
CAS:
362-75-4
| Molecular Weight: | 307.31 g./mol | Molecular Formula: | C₁₃H₁₇N₅O₄ |
|---|---|---|---|
| EC Number: | 206-650-3 | MDL Number: | MFCD00005756 |
| Melting Point: | 221-222 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in biochemical research, this compound serves as a key intermediate in the synthesis of modified nucleosides and nucleotides. It is particularly valuable in the development of antiviral and anticancer agents due to its ability to be incorporated into nucleic acids. Additionally, it plays a role in studying enzyme mechanisms and nucleic acid interactions, aiding in the exploration of cellular processes and drug design. Its isopropylidene protecting group allows for selective chemical modifications, making it a versatile tool in organic synthesis and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Powder Or Crystals |
| Purity (HPLC) | 98-100 |
| Melting Point | 220-225 |
| Infrared Spectrum | Conforms To Structure |
| Specific Rotation [a]20/D(C=1, Dioxane) | -95.5--110 |
| Water By Karl Fischer | 0-1 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $21.60 |
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| 25.000 | 10-20 days | $91.58 |
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| 100.000 | 10-20 days | $338.61 |
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2’,3’-O-Isopropylideneadenosine
Used primarily in biochemical research, this compound serves as a key intermediate in the synthesis of modified nucleosides and nucleotides. It is particularly valuable in the development of antiviral and anticancer agents due to its ability to be incorporated into nucleic acids. Additionally, it plays a role in studying enzyme mechanisms and nucleic acid interactions, aiding in the exploration of cellular processes and drug design. Its isopropylidene protecting group allows for selective chemical modifications, making it a versatile tool in organic synthesis and medicinal chemistry.
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