2-(2-(3-chlorophenyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 162454
| Molecular Weight: | 278.58 g./mol | Molecular Formula: | C₁₅H₂₀BClO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable in constructing complex organic molecules. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable and compatible with a range of functional groups, it supports efficient and selective transformations in both research and industrial settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | colorless liquid |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €601.11 |
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| 5.000 | 10-20 days | €1,373.97 |
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2-(2-(3-chlorophenyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable in constructing complex organic molecules. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable and compatible with a range of functional groups, it supports efficient and selective transformations in both research and industrial settings.
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| Stable in pH range | - |
| Solubility | - |
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| INCI | - |
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