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

blur_circular Chemical Specifications

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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿10,820.00
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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