Bicyclo[4.2.0]octa-1,3,5-trien-3-ylboronic acid
98%
Reagent
Code: #123155
CAS Number
195730-31-5
science Other reagents with same CAS 195730-31-5
blur_circular Chemical Specifications
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Molecular Information
Weight
147.97 g/mol
Formula
C₈H₉BO₂
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Registry Numbers
MDL Number
MFCD09842340
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Physical Properties
Boiling Point
328.5°C at 760 mmHg
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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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