(5-Aminopyridin-3-yl)boronic acid
97%
Reagent
Code: #89355
CAS Number
1169748-84-8
blur_circular Chemical Specifications
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Molecular Information
Weight
137.93 g/mol
Formula
C₅H₇BN₂O₂
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Registry Numbers
MDL Number
MFCD07374883
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Storage & Handling
Storage
-20°C, protected from light, stored under inert gas
description Product Description
(5-Aminopyridin-3-yl)boronic acid is widely utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of various pharmaceuticals, enabling the construction of complex molecular structures. It is also employed in the development of biologically active compounds, including potential drug candidates, due to its ability to interact with specific biological targets. Additionally, it finds use in material science for the synthesis of advanced organic materials and polymers. Its boronic acid group is instrumental in sensing applications, particularly in the detection of sugars and other diol-containing molecules, making it valuable in analytical chemistry and biochemical research.
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(5-Aminopyridin-3-yl)boronic acid
(5-Aminopyridin-3-yl)boronic acid is widely utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of various pharmaceuticals, enabling the construction of complex molecular structures. It is also employed in the development of biologically active compounds, including potential drug candidates, due to its ability to interact with specific biological targets. Additionally, it finds use in material science for the synthesis of advanced organic materials and polymers. Its boronic acid group is instrumental in sensing applications, particularly in the detection of sugars and other diol-containing molecules, making it valuable in analytical chemistry and biochemical research.
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