(5-Aminopyridin-3-yl)boronic acid

97%

Reagent Code: #89355
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CAS Number 1169748-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.93 g/mol
Formula C₅H₇BN₂O₂
badge Registry Numbers
MDL Number MFCD07374883
inventory_2 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,077.00
inventory 250mg
10-20 days ฿6,129.00
inventory 1g
10-20 days ฿13,059.00
(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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