3-Quinolineboronic acid pinacol ester

95%

Reagent Code: #90132
label
Alias 3-Quinolineboronic acid pinacol ester Quinoline-3-boronic acid pinacol ester
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CAS Number 171364-85-5

science Other reagents with same CAS 171364-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.12 g/mol
Formula C₁₅H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD05155218
thermostat Physical Properties
Melting Point 56-60 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of complex organic molecules, particularly in pharmaceutical research. It is employed in the development of drug candidates, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and light-emitting diodes (LEDs), due to its ability to introduce quinoline moieties into larger structures. Its stability and reactivity make it a valuable tool in medicinal chemistry and material science applications.

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Test Parameter Specification
Purity (HPLC) 95-100%
Appearance White to off-white powder or solid or chunks
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿920.00
inventory 5g
10-20 days ฿2,760.00
inventory 25g
10-20 days ฿12,980.00

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3-Quinolineboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of complex organic molecules, particularly in pharmaceutical research. It is employed in the development of drug candidates, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and light-emitting diodes (LEDs), due to its ability to introduce quinoline moieties into larger structures. Its stability and reactivity make it a valuable tool in medicinal chemistry and material science applications.
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