5-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxazole

95%

Reagent Code: #131111
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CAS Number 1403469-16-8

science Other reagents with same CAS 1403469-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.12 g/mol
Formula C₁₅H₁₈BNO₃
badge Registry Numbers
MDL Number MFCD31635744
thermostat Physical Properties
Boiling Point 412.0±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. Commonly employed to construct biaryl and heteroaryl frameworks found in bioactive compounds. Also applied in the development of organic electronic materials due to its ability to link aromatic systems efficiently.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,900.00
inventory 1g
10-20 days ฿45,000.00

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5-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. Commonly employed to construct biaryl and heteroaryl frameworks found in bioactive compounds. Also applied in the development of organic electronic materials due to its ability to lin

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. Commonly employed to construct biaryl and heteroaryl frameworks found in bioactive compounds. Also applied in the development of organic electronic materials due to its ability to link aromatic systems efficiently.

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