6-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-((triisopropylsilyl)ethynyl)naphthalen-2-amine
95%
- Product Code: 186606
CAS:
2820116-32-1
| Molecular Weight: | 467.5 g./mol | Molecular Formula: | C₂₇H₃₉BFNO₂Si |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and materials science research. Its boronate ester group enables efficient carbon-carbon bond formation, while the silyl-protected ethynyl group allows for further functionalization via deprotection and coupling. The fluorine and amine substituents provide additional sites for modification, making it valuable in the development of fluorinated bioactive compounds and conjugated organic materials such as OLEDs or sensors. Its design supports high reactivity and selectivity in multi-step synthetic pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿13,680.00 |
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| 0.250 | 10-20 days | ฿23,270.00 |
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| 1.000 | 10-20 days | ฿60,500.00 |
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6-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-((triisopropylsilyl)ethynyl)naphthalen-2-amine
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and materials science research. Its boronate ester group enables efficient carbon-carbon bond formation, while the silyl-protected ethynyl group allows for further functionalization via deprotection and coupling. The fluorine and amine substituents provide additional sites for modification, making it valuable in the development of fluorinated bioactive compounds and conjugated organic materials such as OLEDs or sensors. Its design supports high reactivity and selectivity in multi-step synthetic pathways.
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