4-Ethyl-2-phenyl-1,3,2-dioxaborolane

98%

Reagent Code: #46778
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CAS Number 53774-64-4

science Other reagents with same CAS 53774-64-4

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Weight 176.02 g/mol
Formula C₁₀H₁₃BO₂
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This chemical is primarily utilized in organic synthesis as a boron-containing reagent. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds, particularly in the synthesis of complex organic molecules like pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable arylboronic ester, which serves as a key precursor in various catalytic processes. Additionally, it finds use in the development of sensors and polymers, where boron-based compounds play a crucial role in enhancing material properties.

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inventory 1g
10-20 days ฿729.00

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4-Ethyl-2-phenyl-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis as a boron-containing reagent. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds, particularly in the synthesis of complex organic molecules like pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable arylboronic ester, which serves as a key precursor in various catalytic processes. Additionally, it finds use in the development of sensor

This chemical is primarily utilized in organic synthesis as a boron-containing reagent. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds, particularly in the synthesis of complex organic molecules like pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable arylboronic ester, which serves as a key precursor in various catalytic processes. Additionally, it finds use in the development of sensors and polymers, where boron-based compounds play a crucial role in enhancing material properties.

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