(1S,2S,3S,5S)-5-(2-Amino-6-(benzyloxy)-9H-purin-9-yl)-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol
97%
- Product Code: 113031
CAS:
142217-77-4
| Molecular Weight: | 551.64 g./mol | Molecular Formula: | C₃₂H₃₃N₅O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09750977 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of multiple benzyloxy groups and the purine moiety makes it a versatile building block for modifying nucleoside structures to enhance their biological activity and selectivity. Researchers often employ it in the design of prodrugs, aiming to improve drug delivery and efficacy. Additionally, its stereochemistry plays a significant role in ensuring the desired pharmacological properties of the final compounds. This chemical is particularly valuable in the development of treatments targeting viral infections and certain types of cancer.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿774.00 |
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| 1.000 | 10-20 days | ฿2,664.00 |
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| 5.000 | 10-20 days | ฿8,838.00 |
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(1S,2S,3S,5S)-5-(2-Amino-6-(benzyloxy)-9H-purin-9-yl)-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of multiple benzyloxy groups and the purine moiety makes it a versatile building block for modifying nucleoside structures to enhance their biological activity and selectivity. Researchers often employ it in the design of prodrugs, aiming to improve drug delivery and efficacy. Additionally, its stereochemistry plays a significant role in ensuring the desired pharmacological properties of the final compounds. This chemical is particularly valuable in the development of treatments targeting viral infections and certain types of cancer.
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