(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid

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Reagent Code: #113362
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CAS Number 1000269-51-1

science Other reagents with same CAS 1000269-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.05 g/mol
Formula C₁₃H₁₂BNO₄
badge Registry Numbers
MDL Number MFCD16038213
thermostat Physical Properties
Boiling Point 495.051 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.312 g/cm3
Storage 2-8°C, inert gas

description Product Description

(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules, including potential drug candidates. The boronic acid group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in many bioactive compounds. Additionally, it can be used in the development of materials science, particularly in the synthesis of organic electronic materials. Its role in these applications highlights its importance in advancing both medicinal chemistry and material innovation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿9,000.00

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(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid
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(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules, including potential drug candidates. The boronic acid group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in many bioactive compounds. Additionally, it can be used in the development of materials science, particularly in the synthesis of organic electronic materials. Its role in these applications highlights its importance in advancing both medicinal chemistry and material innovation.
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