(3-Fluoro-5-(isopropoxymethyl)phenyl)boronic acid

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Reagent Code: #90171
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CAS Number 1704063-75-1
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Weight 212.03 g/mol
Formula C₁₀H₁₄BFO₃
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MDL Number MFCD23751359
inventory_2 Storage & Handling
Storage  2-8°C

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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds applications in material science for synthesizing advanced polymers and organic electronic materials. The fluorine substituent enhances its reactivity and stability, making it suitable for precise and efficient chemical transformations.

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inventory 500mg
10-20 days ฿17,442.00

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(3-Fluoro-5-(isopropoxymethyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds applications in material science for synthesizing advanced polymers and organic electro

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds applications in material science for synthesizing advanced polymers and organic electronic materials. The fluorine substituent enhances its reactivity and stability, making it suitable for precise and efficient chemical transformations.

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