trans-2-(4-Chlorophenyl)vinylboronic acid

95%

Reagent Code: #91110
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CAS Number 154230-29-2

science Other reagents with same CAS 154230-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.41 g/mol
Formula C₈H₈BClO₂
badge Registry Numbers
MDL Number MFCD02093767
thermostat Physical Properties
Melting Point 165°C-分解
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure allows it to act as a versatile intermediate in the synthesis of complex organic compounds, including biologically active molecules and polymers. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to facilitate the creation of conjugated systems. Its stability and reactivity make it a useful tool in medicinal chemistry for designing and optimizing drug candidates.

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inventory 1g
10-20 days ฿6,912.00

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trans-2-(4-Chlorophenyl)vinylboronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure allows it to act as a versatile intermediate in the synthesis of complex organic compounds, including biologically active molecules and polymers. Additionally, it is employed in the development of organic electronic materials

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure allows it to act as a versatile intermediate in the synthesis of complex organic compounds, including biologically active molecules and polymers. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to facilitate the creation of conjugated systems. Its stability and reactivity make it a useful tool in medicinal chemistry for designing and optimizing drug candidates.

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