1,3,2-Dioxaborolane, 2-(9,9-Dimethyl-9H-Fluoren-2-YL)-4,4,5,5-Tetramethyl
≥98%
- Product Code: 91199
CAS:
569343-09-5
Molecular Weight: | 320.24 g./mol | Molecular Formula: | C₂₁H₂₅BO₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its ability to enhance charge transport properties. Its stability and reactivity also make it a preferred choice in polymer chemistry for creating functionalized polymers with tailored properties.
Product Specification:
Test | Specification |
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APPEARANCE | White - Almost white Crystal - Powder |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | $15.07 |
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1.000 | 10-20 days | $30.14 |
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5.000 | 10-20 days | $91.41 |
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25.000 | 10-20 days | $411.85 |
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1,3,2-Dioxaborolane, 2-(9,9-Dimethyl-9H-Fluoren-2-YL)-4,4,5,5-Tetramethyl
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its ability to enhance charge transport properties. Its stability and reactivity also make it a preferred choice in polymer chemistry for creating functionalized polymers with tailored properties.
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