4,4,5,5-tetramethyl-2-(2-(m-tolyl)prop-1-en-1-yl)-1,3,2-dioxaborolane
98%
- Product Code: 242176
CAS:
1398771-23-7
| Molecular Weight: | 258.17 g./mol | Molecular Formula: | C₁₆H₂₃BO₂ |
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| 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 organic synthesis. Its boron-containing structure allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, facilitating the construction of biaryl and conjugated systems important in pharmaceuticals, agrochemicals, and advanced materials. The presence of the m-tolyl group makes it valuable for introducing meta-substituted aromatic motifs into larger molecules. Stable and compatible with a variety of functional groups, it is particularly useful in late-stage functionalization during drug development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | Ft34,815.68 |
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| 1.000 | 10-20 days | Ft243,918.88 |
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| 5.000 | 10-20 days | Ft571,688.15 |
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4,4,5,5-tetramethyl-2-(2-(m-tolyl)prop-1-en-1-yl)-1,3,2-dioxaborolane
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, facilitating the construction of biaryl and conjugated systems important in pharmaceuticals, agrochemicals, and advanced materials. The presence of the m-tolyl group makes it valuable for introducing meta-substituted aromatic motifs into larger molecules. Stable and compatible with a variety of functional groups, it is particularly useful in late-stage functionalization during drug development.
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