2-(2-(4-chloro)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
99%
- Product Code: 162453
CAS:
1187525-05-8
| Molecular Weight: | 278.58 g./mol | Molecular Formula: | C₁₅H₂₀BClO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boron-containing structure allows for efficient and selective coupling with aryl or vinyl halides under palladium catalysis. Commonly applied in the preparation of complex organic molecules, including active pharmaceutical ingredients and functional materials. Stable and compatible with a variety of functional groups, making it valuable in late-stage functionalization during drug development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | pale yellow oil |
| Purity (%) | 99-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $152.81 |
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| 1.000 | 10-20 days | $700.13 |
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| 5.000 | 10-20 days | $1,675.31 |
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2-(2-(4-chloro)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boron-containing structure allows for efficient and selective coupling with aryl or vinyl halides under palladium catalysis. Commonly applied in the preparation of complex organic molecules, including active pharmaceutical ingredients and functional materials. Stable and compatible with a variety of functional groups, making it valuable in late-stage functionalization during drug development.
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| Stable in pH range | - |
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| INCI | - |
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