Bicyclo[4.2.0]octa-1,3,5-trien-3-ylboronic acid

98%

Reagent Code: #123155
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CAS Number 195730-31-5

science Other reagents with same CAS 195730-31-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.97 g/mol
Formula C₈H₉BO₂
badge Registry Numbers
MDL Number MFCD09842340
thermostat Physical Properties
Boiling Point 328.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules, particularly in cross-coupling reactions. It is often employed in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds, due to its boronic acid functional group. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bicyclic structure can impart unique steric and electronic properties, making it valuable in the development of novel compounds with specific biological or chemical activities. Its application extends to materials science, where it contributes to the creation of organic electronic materials and polymers.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,553.00
inventory 250mg
10-20 days ฿2,187.00
inventory 100mg
10-20 days ฿1,323.00

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Bicyclo[4.2.0]octa-1,3,5-trien-3-ylboronic acid
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This compound is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules, particularly in cross-coupling reactions. It is often employed in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds, due to its boronic acid functional group. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bicyclic structure can impart unique steric and electronic properties, making it valuable in the development of novel compounds with specific biological or chemical activities. Its application extends to materials science, where it contributes to the creation of organic electronic materials and polymers.
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