4,4,5,5-Tetramethyl-2-(oct-1-en-1-yl)-1,3,2-dioxaborolane
≥95%
- Product Code: 244101
CAS:
170942-79-7
Molecular Weight: | 238.18 g./mol | Molecular Formula: | C₁₄H₂₇BO₂ |
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EC Number: | MDL Number: | MFCD03453667 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry, inert gas |
Product Description:
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce alkenyl groups into aromatic or heteroaromatic systems, enabling the formation of carbon-carbon bonds. The presence of the oct-1-enyl chain allows for further functionalization or incorporation of long hydrophobic segments in target molecules, making it valuable in the synthesis of specialty organic compounds, including intermediates for pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity profile make it suitable for use in both laboratory-scale and industrial applications where selective and efficient coupling is required.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.250 | 10-20 days | $86.92 |
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1.000 | 10-20 days | $238.14 |
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5.000 | 10-20 days | $975.18 |
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4,4,5,5-Tetramethyl-2-(oct-1-en-1-yl)-1,3,2-dioxaborolane
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce alkenyl groups into aromatic or heteroaromatic systems, enabling the formation of carbon-carbon bonds. The presence of the oct-1-enyl chain allows for further functionalization or incorporation of long hydrophobic segments in target molecules, making it valuable in the synthesis of specialty organic compounds, including intermediates for pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity profile make it suitable for use in both laboratory-scale and industrial applications where selective and efficient coupling is required.
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