1,1,1,3,3,3-Hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol

98%

Reagent Code: #197581
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CAS Number 449804-09-5

science Other reagents with same CAS 449804-09-5

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scatter_plot Molecular Information
Weight 370.10 g/mol
Formula C₁₅H₁₇BF₆O₃
badge Registry Numbers
MDL Number MFCD22570625
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing bioactive molecules with enhanced metabolic stability and lipophilicity. The presence of hexafluoroisopropanol moiety imparts strong electron-withdrawing properties, useful in materials science for tuning electronic properties of organic semiconductors and functional polymers. Commonly employed in the preparation of fluorinated liquid crystals and advanced specialty chemicals.

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inventory 100mg
10-20 days ฿10,820.00

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1,1,1,3,3,3-Hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing bioactive molecules with enhanced metabolic stability and lipophilicity. The presence of hexafluoroisopropanol moiety imparts strong electron-withdrawing properties, useful in materials science for tuning electronic properties o

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing bioactive molecules with enhanced metabolic stability and lipophilicity. The presence of hexafluoroisopropanol moiety imparts strong electron-withdrawing properties, useful in materials science for tuning electronic properties of organic semiconductors and functional polymers. Commonly employed in the preparation of fluorinated liquid crystals and advanced specialty chemicals.

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