(R)-()-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolane
98%
- Product Code: 230016
CAS:
57044-24-3
| Molecular Weight: | 150.6 g./mol | Molecular Formula: | C₆H₁₁ClO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00273371 | |
| Melting Point: | Boiling Point: | 63°C 37mm Hg (Lit.) | |
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its structure allows for selective functionalization, making it valuable in asymmetric synthesis. Commonly employed in the preparation of β-blockers and other cardiovascular drugs due to its ability to introduce a chiral 1,2-diol motif. Also utilized in agrochemicals for the development of enantiomerically pure pesticides and herbicides. The chloromethyl group serves as a reactive handle for further chemical transformations, enabling coupling reactions with nucleophiles such as amines or thiols.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $12.34 |
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| 5.000 | 10-20 days | $20.86 |
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| 25.000 | 10-20 days | $95.77 |
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| 100.000 | 10-20 days | $382.24 |
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(R)-()-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolane
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its structure allows for selective functionalization, making it valuable in asymmetric synthesis. Commonly employed in the preparation of β-blockers and other cardiovascular drugs due to its ability to introduce a chiral 1,2-diol motif. Also utilized in agrochemicals for the development of enantiomerically pure pesticides and herbicides. The chloromethyl group serves as a reactive handle for further chemical transformations, enabling coupling reactions with nucleophiles such as amines or thiols.
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