(Difluoromethyl)trimethylsilane
97%
- Product Code: 88029
CAS:
65864-64-4
| Molecular Weight: | 124.21 g./mol | Molecular Formula: | C₄H₁₀F₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19381658 | |
| Melting Point: | Boiling Point: | 52°C | |
| Density: | 0.91g/mL | Storage Condition: | 2-8°C, inert gas storage |
Product Description:
(Difluoromethyl)trimethylsilane is primarily utilized in organic synthesis as a versatile reagent for introducing the difluoromethyl group into various molecules. This functional group is particularly valuable in pharmaceutical and agrochemical research due to its ability to enhance the metabolic stability and bioavailability of compounds. It is often employed in nucleophilic substitution reactions, where it acts as a difluoromethylating agent, enabling the synthesis of difluoromethylated aromatic and heteroaromatic compounds. Additionally, it finds application in the preparation of advanced materials, such as fluorinated polymers, which exhibit unique properties like chemical resistance and thermal stability. Its use in cross-coupling reactions further extends its utility in constructing complex molecular architectures for drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to light yellow liquid |
| PURITY | 96.5-100 |
| REFRACTIVE INDEX N20D | 1.356-1.36 |
| Infrared spectrum | Conforms to Structure |
| Specific gravity 2020C | 0.908-0.912 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $58.60 |
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| 25.000 | 10-20 days | $259.55 |
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(Difluoromethyl)trimethylsilane
(Difluoromethyl)trimethylsilane is primarily utilized in organic synthesis as a versatile reagent for introducing the difluoromethyl group into various molecules. This functional group is particularly valuable in pharmaceutical and agrochemical research due to its ability to enhance the metabolic stability and bioavailability of compounds. It is often employed in nucleophilic substitution reactions, where it acts as a difluoromethylating agent, enabling the synthesis of difluoromethylated aromatic and heteroaromatic compounds. Additionally, it finds application in the preparation of advanced materials, such as fluorinated polymers, which exhibit unique properties like chemical resistance and thermal stability. Its use in cross-coupling reactions further extends its utility in constructing complex molecular architectures for drug discovery and development.
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