(4-Chlorophenyl)vinylboronic acid pinacol ester

95%

Reagent Code: #90646
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CAS Number 223919-54-8

science Other reagents with same CAS 223919-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.556 g/mol
Formula C₁₄H₁₈BClO₂
badge Registry Numbers
MDL Number MFCD15144834
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

(4-Chlorophenyl)vinylboronic acid pinacol ester is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, polymers, and advanced materials. Additionally, it is employed in the development of functionalized styrene derivatives, which are essential intermediates in various chemical processes. Its stability and reactivity under mild conditions make it a preferred choice for researchers and industrial chemists.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,926.00
inventory 1g
10-20 days ฿5,157.00
inventory 5g
10-20 days ฿21,096.00

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(4-Chlorophenyl)vinylboronic acid pinacol ester
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(4-Chlorophenyl)vinylboronic acid pinacol ester is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, polymers, and advanced materials. Additionally, it is employed in the development of functionalized styrene derivatives, which are essential intermediates in various chemical processes. Its stability and reactivity under mild conditions make it a preferred choice for researchers and industrial chemists.
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