(2-((3-Methylbenzyl)oxy)phenyl)boronic acid

95%

Reagent Code: #41526
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CAS Number 1311163-93-5

science Other reagents with same CAS 1311163-93-5

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Weight 242.08 g/mol
Formula C₁₄H₁₅BO₃
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description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it can be employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its stability and reactivity also make it a suitable candidate for research in medicinal chemistry, particularly in the design of bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,393.00
inventory 250mg
10-20 days ฿7,600.00
inventory 1g
10-20 days ฿20,020.00

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(2-((3-Methylbenzyl)oxy)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it can be employed in the development of sensors and probes due to its

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it can be employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its stability and reactivity also make it a suitable candidate for research in medicinal chemistry, particularly in the design of bioactive compounds.

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