1-[4-(4,4,6-Trimethyl-1,3,2-dioxaborinan-2-yl)phenyl]ethan-1-one

≥95%

Reagent Code: #244716
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CAS Number 934558-34-6

science Other reagents with same CAS 934558-34-6

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scatter_plot Molecular Information
Weight 246.11 g/mol
Formula C₁₄H₁₉BO₃
badge Registry Numbers
MDL Number MFCD28101504
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boron-containing group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The ketone functionality allows for further derivatization, such as reduction or condensation reactions, expanding its utility in building bioactive structures. Commonly employed in medicinal chemistry for constructing drug-like scaffolds, especially in the development of aromatic ketone derivatives with targeted biological activity.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿5,990.00
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1-[4-(4,4,6-Trimethyl-1,3,2-dioxaborinan-2-yl)phenyl]ethan-1-one
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boron-containing group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The ketone functionality allows for further derivatization, such as reduction or condensation reactions, expanding its utility in building bioactive structu

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boron-containing group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The ketone functionality allows for further derivatization, such as reduction or condensation reactions, expanding its utility in building bioactive structures. Commonly employed in medicinal chemistry for constructing drug-like scaffolds, especially in the development of aromatic ketone derivatives with targeted biological activity.

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