(4-(trans-4-propylcyclohexyl)phenyl)boronic acid

95%

Reagent Code: #91114
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CAS Number 146862-02-4

science Other reagents with same CAS 146862-02-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.15 g/mol
Formula C₁₅H₂₃BO₂
thermostat Physical Properties
Boiling Point 394.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the preparation of liquid crystal materials due to its cyclohexylphenyl structure, which contributes to the desired mesomorphic properties. Its role in catalysis and material science further highlights its versatility in research and industrial processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿1,610.00
inventory 25g
10-20 days ฿6,320.00

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(4-(trans-4-propylcyclohexyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the preparation of liquid crystal materials due to its cyclohexyl

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the preparation of liquid crystal materials due to its cyclohexylphenyl structure, which contributes to the desired mesomorphic properties. Its role in catalysis and material science further highlights its versatility in research and industrial processes.

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