2-(2-cyclopropylprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
99%
- Product Code: 162452
CAS:
2246919-45-7
| Molecular Weight: | 208.11 g./mol | Molecular Formula: | C₁₂H₂₁BO₂ |
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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 complex organic synthesis. Its boron-containing structure allows efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical development. The cyclopropyl group enhances steric and electronic properties, improving selectivity and yield in certain transformations. Commonly employed in late-stage functionalization due to its stability and reactivity profile.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | colorless liquid |
| Purity (%) | 99-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,540.00 |
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| 0.250 | 10-20 days | ฿7,700.00 |
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| 1.000 | 10-20 days | ฿24,300.00 |
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| 5.000 | 10-20 days | ฿60,750.00 |
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2-(2-cyclopropylprop-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 complex organic synthesis. Its boron-containing structure allows efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical development. The cyclopropyl group enhances steric and electronic properties, improving selectivity and yield in certain transformations. Commonly employed in late-stage functionalization due to its stability and reactivity profile.
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| Stable in pH range | - |
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| INCI | - |
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