B-[4-[[(2-thienylmethyl)amino]carbonyl]phenyl]Boronic acid
95%
Reagent
Code: #90357
CAS Number
874460-04-5
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Molecular Information
Weight
261.10458 g/mol
Formula
C₁₂H₁₂BNO₃S
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Registry Numbers
MDL Number
MFCD31648846
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Storage & Handling
Storage
2-8°C
description Product Description
B-[4-[[(2-thienylmethyl)amino]carbonyl]phenyl]Boronic acid is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to construct complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its boronic acid functional group makes it valuable in the design of sensors and probes for detecting biological molecules, such as sugars and other analytes. The compound’s unique structure also contributes to its use in the study of enzyme inhibition and drug discovery, particularly in targeting diseases like cancer and diabetes. Its applications extend to materials science, where it aids in the development of advanced polymers and coatings.
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B-[4-[[(2-thienylmethyl)amino]carbonyl]phenyl]Boronic acid
B-[4-[[(2-thienylmethyl)amino]carbonyl]phenyl]Boronic acid is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to construct complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its boronic acid functional group makes it valuable in the design of sensors and probes for detecting biological molecules, such as sugars and other analytes. The compound’s unique structure also contributes to its use in the study of enzyme inhibition and drug discovery, particularly in targeting diseases like cancer and diabetes. Its applications extend to materials science, where it aids in the development of advanced polymers and coatings.
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