Benzonitrile, 4-[3-[(acetyloxy)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-

95%

Reagent Code: #150145
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CAS Number 2227126-13-6

science Other reagents with same CAS 2227126-13-6

blur_circular Chemical Specifications

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Weight 393.24 g/mol
Formula C₂₂H₂₄BNO₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure supports the construction of biaryl systems found in bioactive compounds and advanced intermediates.

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inventory 100mg
10-20 days ฿28,500.00

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Benzonitrile, 4-[3-[(acetyloxy)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure su

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure supports the construction of biaryl systems found in bioactive compounds and advanced intermediates.

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