(4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol 4,5-Bis(4-methylbenzenesulfonate)
≥95%
- Product Code: 70928
CAS:
51064-65-4
| Molecular Weight: | 470.6 g./mol | Molecular Formula: | C₂₁H₂₆O₈S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 90-92°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a chiral building block for the production of complex molecules. Its structure, featuring two tosylate groups, makes it highly reactive in nucleophilic substitution reactions, enabling the formation of chiral intermediates. These intermediates are crucial in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs, where stereochemistry plays a key role in efficacy and safety. Additionally, it is employed in the preparation of advanced materials, such as liquid crystals and polymers, where precise control over molecular architecture is required. Its application extends to research settings, where it serves as a valuable reagent for studying stereoselective reactions and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,890.00 |
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| 5.000 | 10-20 days | ฿7,250.00 |
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(4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol 4,5-Bis(4-methylbenzenesulfonate)
This chemical is primarily utilized in organic synthesis as a chiral building block for the production of complex molecules. Its structure, featuring two tosylate groups, makes it highly reactive in nucleophilic substitution reactions, enabling the formation of chiral intermediates. These intermediates are crucial in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs, where stereochemistry plays a key role in efficacy and safety. Additionally, it is employed in the preparation of advanced materials, such as liquid crystals and polymers, where precise control over molecular architecture is required. Its application extends to research settings, where it serves as a valuable reagent for studying stereoselective reactions and developing new synthetic methodologies.
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