2,2',2''-(2,4,6-Trifluorobenzene-1,3,5-triyl)tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
98%
- Product Code: 243521
CAS:
408492-24-0
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| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules with fluorinated aromatic cores. Its boronate ester groups allow for efficient and selective formation of carbon-carbon bonds, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful in constructing conjugated systems for optoelectronic materials due to the electron-withdrawing nature of the trifluorobenzene ring. Stable and compatible with a wide range of functional groups, it supports modular and scalable synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $136.62 |
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| 0.250 | 10-20 days | $248.31 |
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| 1.000 | 10-20 days | $628.57 |
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| 5.000 | 10-20 days | $2,175.58 |
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2,2',2''-(2,4,6-Trifluorobenzene-1,3,5-triyl)tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules with fluorinated aromatic cores. Its boronate ester groups allow for efficient and selective formation of carbon-carbon bonds, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful in constructing conjugated systems for optoelectronic materials due to the electron-withdrawing nature of the trifluorobenzene ring. Stable and compatible with a wide range of functional groups, it supports modular and scalable synthetic routes.
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