2-Methoxy-4-(2-methylimidazol-1-yl)phenylboronic acid
95%
Reagent
Code: #91708
CAS Number
2225169-63-9
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Molecular Information
Weight
232.04352 g/mol
Formula
C₁₁H₁₃BN₂O₃
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Storage & Handling
Storage
-20℃
description Product Description
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, its imidazole moiety can contribute to interactions with biological targets, making it useful in medicinal chemistry research for designing enzyme inhibitors or receptor modulators. Its applications also extend to the synthesis of fluorescent dyes and polymers, where its structural properties enhance functionality and stability.
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2-Methoxy-4-(2-methylimidazol-1-yl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, its imidazole moiety can contribute to interactions with biological targets, making it useful in medicinal chemistry research for designing enzyme inhibitors or receptor modulators. Its applications also extend to the synthesis of fluorescent dyes and polymers, where its structural properties enhance functionality and stability.
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