(R)-2-(bromomethyl)-2,3-dihydrobenzo[b][1,4]dioxine
≥95%
- Product Code: 37516
CAS:
1142953-55-6
| Molecular Weight: | 229.07 g./mol | Molecular Formula: | C₉H₉BrO₂ |
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| Melting Point: | Boiling Point: | 288.3±19.0℃(Predicted) | |
| Density: | 1.501±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmacologically active molecules. Its structure, featuring a bromomethyl group attached to a dihydrobenzo[d][1,4]dioxine ring, makes it a valuable building block in the development of chiral compounds, particularly in asymmetric synthesis. It is often employed in the synthesis of ligands and catalysts used in enantioselective reactions, which are crucial in producing drugs with high stereochemical purity. Additionally, it finds application in the creation of complex heterocyclic compounds that are explored for their potential biological activities, such as antimicrobial, anticancer, or central nervous system-targeting agents. Its reactivity allows for further functionalization, enabling the construction of diverse molecular frameworks in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,903.10 |
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(R)-2-(bromomethyl)-2,3-dihydrobenzo[b][1,4]dioxine
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmacologically active molecules. Its structure, featuring a bromomethyl group attached to a dihydrobenzo[d][1,4]dioxine ring, makes it a valuable building block in the development of chiral compounds, particularly in asymmetric synthesis. It is often employed in the synthesis of ligands and catalysts used in enantioselective reactions, which are crucial in producing drugs with high stereochemical purity. Additionally, it finds application in the creation of complex heterocyclic compounds that are explored for their potential biological activities, such as antimicrobial, anticancer, or central nervous system-targeting agents. Its reactivity allows for further functionalization, enabling the construction of diverse molecular frameworks in medicinal chemistry research.
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