(2R,3R,4R)-3,4-Bis(benzyloxy)-2-((benzyloxy)methyl)-5-methoxytetrahydrofuran
≥95%
- Product Code: 40113
CAS:
64363-77-5
| Molecular Weight: | 434.52 g./mol | Molecular Formula: | C₂₇H₃₀O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23704947 | |
| Melting Point: | Boiling Point: | 552.6±50.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of carbohydrate chemistry. It serves as a key intermediate in the preparation of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its structure, featuring multiple benzyloxy groups, allows for selective protection and deprotection during multi-step synthetic processes. Additionally, it is employed in the production of modified sugars and glycoconjugates, which are essential for studying biological processes and designing therapeutic agents. Its role in asymmetric synthesis also makes it valuable for creating enantiomerically pure compounds in pharmaceutical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,951.00 |
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| 0.250 | 10-20 days | ฿6,588.00 |
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| 1.000 | 10-20 days | ฿19,782.00 |
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(2R,3R,4R)-3,4-Bis(benzyloxy)-2-((benzyloxy)methyl)-5-methoxytetrahydrofuran
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of carbohydrate chemistry. It serves as a key intermediate in the preparation of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its structure, featuring multiple benzyloxy groups, allows for selective protection and deprotection during multi-step synthetic processes. Additionally, it is employed in the production of modified sugars and glycoconjugates, which are essential for studying biological processes and designing therapeutic agents. Its role in asymmetric synthesis also makes it valuable for creating enantiomerically pure compounds in pharmaceutical research.
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