2-(Bromomethyl)benzeneboronic acid neopentyl glycol ester

95%

Reagent Code: #89893
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CAS Number 441011-76-3

science Other reagents with same CAS 441011-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.97 g/mol
Formula C₁₂H₁₆BBrO₂
badge Registry Numbers
MDL Number MFCD04039022
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a versatile boronic ester reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable intermediate in the preparation of aryl and heteroaryl compounds. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various functional groups. Its application extends to polymer chemistry, where it is used to modify and functionalize polymeric materials for specific industrial purposes.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,367.00
inventory 1g
10-20 days ฿9,261.00

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2-(Bromomethyl)benzeneboronic acid neopentyl glycol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a versatile boronic ester reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable intermediate in the preparation of aryl and heteroaryl compounds. Additionally, it is employed in the development of sen

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a versatile boronic ester reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable intermediate in the preparation of aryl and heteroaryl compounds. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various functional groups. Its application extends to polymer chemistry, where it is used to modify and functionalize polymeric materials for specific industrial purposes.

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