(2-Oxo-2H-chromen-7-yl)boronic acid

98%

Reagent Code: #222492
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CAS Number 1357078-03-5

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blur_circular Chemical Specifications

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Weight 189.96 g/mol
Formula C₉H₇BO₄
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of coumarin-based compounds with biological activity, particularly in pharmaceuticals and agrochemicals. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds in drug development. Commonly employed in the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the coumarin scaffold. Also applied in materials science for designing organic semiconductors and luminescent materials.

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inventory 10mg
10-20 days ฿5,110.00

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(2-Oxo-2H-chromen-7-yl)boronic acid
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Used as a key intermediate in the synthesis of coumarin-based compounds with biological activity, particularly in pharmaceuticals and agrochemicals. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds in drug development. Commonly employed in the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the coumarin scaffold. Also applied in materials science for designing organic semiconducto

Used as a key intermediate in the synthesis of coumarin-based compounds with biological activity, particularly in pharmaceuticals and agrochemicals. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds in drug development. Commonly employed in the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the coumarin scaffold. Also applied in materials science for designing organic semiconductors and luminescent materials.

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