(2-Methoxyquinolin-7-yl)boronic acid

98%

Reagent Code: #131592
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CAS Number 2377608-28-9

science Other reagents with same CAS 2377608-28-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203 g/mol
Formula C₁₀H₁₀BNO₃
badge Registry Numbers
MDL Number MFCD22394149
thermostat Physical Properties
Boiling Point 405.2±48.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its quinoline core with a methoxy group enhances electronic properties useful in designing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and fluorescent probes due to the quinoline scaffold’s affinity for biological targets and optical activity. The boronic acid functionality allows for rapid derivatization, making it valuable in medicinal chemistry and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,910.00
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,300.00

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(2-Methoxyquinolin-7-yl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its quinoline core with a methoxy group enhances electronic properties useful in designing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and fluorescent probes due to the quinoline scaffold’s affinity for biological targets and optical activity. The boronic acid functionality allows for rapi

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its quinoline core with a methoxy group enhances electronic properties useful in designing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and fluorescent probes due to the quinoline scaffold’s affinity for biological targets and optical activity. The boronic acid functionality allows for rapid derivatization, making it valuable in medicinal chemistry and materials science.

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