(2R,3R,4S,5S)-2-((Benzoyloxy)methyl)-5-methoxytetrahydrofuran-3,4-diyl dibenzoate
98%
- Product Code: 230743
CAS:
7473-42-9
| Molecular Weight: | 476.47 g./mol | Molecular Formula: | C₂₇H₂₄O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00057268 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas storage |
Product Description:
Used as a chiral building block in organic synthesis, particularly in the preparation of nucleoside analogs and antiviral agents. Its protected sugar-like structure with multiple stereocenters makes it valuable for constructing complex molecules where stereochemistry is critical. Commonly employed in the pharmaceutical industry for the synthesis of modified ribose derivatives used in drug development, especially in antiviral and anticancer compounds. The benzoate groups serve as protecting groups that can be selectively removed, allowing stepwise functionalization of the sugar ring. Also utilized in research settings for studying glycosylation reactions and enzyme substrates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,720.00 |
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| 5g | 10-20 days | ฿8,020.00 |
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| 10g | 10-20 days | ฿16,020.00 |
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(2R,3R,4S,5S)-2-((Benzoyloxy)methyl)-5-methoxytetrahydrofuran-3,4-diyl dibenzoate
Used as a chiral building block in organic synthesis, particularly in the preparation of nucleoside analogs and antiviral agents. Its protected sugar-like structure with multiple stereocenters makes it valuable for constructing complex molecules where stereochemistry is critical. Commonly employed in the pharmaceutical industry for the synthesis of modified ribose derivatives used in drug development, especially in antiviral and anticancer compounds. The benzoate groups serve as protecting groups that can be selectively removed, allowing stepwise functionalization of the sugar ring. Also utilized in research settings for studying glycosylation reactions and enzyme substrates.
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