2-Methyl-4-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid
95%
Reagent
Code: #91734
CAS Number
2225171-80-0
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Molecular Information
Weight
216.04412 g/mol
Formula
C₁₁H₁₃BN₂O₂
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Storage & Handling
Storage
-20℃
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronic acid functional group enables it to participate in Suzuki-Miyaura reactions, which are widely employed in the formation of carbon-carbon bonds. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its pyrazole moiety can contribute to the development of biologically active molecules, such as enzyme inhibitors or receptor modulators, due to its ability to interact with various biological targets. Its application extends to the field of medicinal chemistry, where it is used to create complex molecular structures for drug discovery and development.
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2-Methyl-4-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronic acid functional group enables it to participate in Suzuki-Miyaura reactions, which are widely employed in the formation of carbon-carbon bonds. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its pyrazole moiety can contribute to the development of biologically active molecules, such as enzyme inhibitors or receptor modulators, due to its ability to interact with various biological targets. Its application extends to the field of medicinal chemistry, where it is used to create complex molecular structures for drug discovery and development.
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