(R)-4-(Iodomethyl)-2,2-dimethyl-1,3-dioxolane
≥95%
- Product Code: 37673
CAS:
23735-39-9
| Molecular Weight: | 242.06 g./mol | Molecular Formula: | C₆H₁₁IO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07367263 | |
| Melting Point: | Boiling Point: | 217.3°C at 760 mmHg | |
| Density: | 1.623g/cm3 | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its iodine moiety makes it a versatile reagent for nucleophilic substitution reactions, enabling the introduction of the dioxolane ring into more complex molecular structures. This is particularly valuable in the synthesis of biologically active compounds, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing the selectivity and efficiency of chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $396.40 |
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| 0.250 | 10-20 days | $693.70 |
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| 1.000 | 10-20 days | $1,733.84 |
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(R)-4-(Iodomethyl)-2,2-dimethyl-1,3-dioxolane
This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its iodine moiety makes it a versatile reagent for nucleophilic substitution reactions, enabling the introduction of the dioxolane ring into more complex molecular structures. This is particularly valuable in the synthesis of biologically active compounds, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing the selectivity and efficiency of chemical transformations.
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