7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole

95%

Reagent Code: #243450
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CAS Number 2137501-14-3

science Other reagents with same CAS 2137501-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.08 g/mol
Formula C₁₃H₁₆NO₃B
badge Registry Numbers
MDL Number MFCD16995817
inventory_2 Storage & Handling
Storage 2-8°C, dry

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 boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is particularly useful in constructing biaryl frameworks found in bioactive compounds and functional materials. Due to the presence of the benzo[d]oxazole moiety, the resulting coupled products often exhibit enhanced photophysical properties, supporting applications in the development of organic light-emitting diodes (OLEDs) and fluorescent sensors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,830.00
inventory 1g
10-20 days ฿7,260.00
inventory 5g
10-20 days ฿25,280.00

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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole
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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 boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is particularly useful in constructing biaryl frameworks found in bioactive compounds and functional materials. Due to the presence of the benzo[d]oxazole moiety, the resulting coupled products often exhibit enhanced photophysical properties, supporting applications in the development of organic light-emitting diodes (OLEDs) and fluorescent sensors.
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