2-(Piperidin-3-yl)-4-chlorophenylboronic acid
95%
Reagent
Code: #62735
CAS Number
2225151-96-0
blur_circular Chemical Specifications
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Molecular Information
Weight
239.5063 g/mol
Formula
C₁₁H₁₅BClNO₂
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Storage & Handling
Storage
-20℃
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 the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is highly reactive with aryl halides in the presence of a palladium catalyst, making it valuable in the pharmaceutical industry for synthesizing drug candidates. Additionally, it is employed in material science for developing advanced polymers and functional materials. Its structural properties also make it suitable for use in biochemical research, particularly in studying enzyme inhibition and receptor binding.
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