(4-Aminophenyl)boronic acid hydrate

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Reagent Code: #132837
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CAS Number 960355-27-5

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blur_circular Chemical Specifications

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Weight 154.96 g/mol
Formula C₆H₁₀BNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals. Commonly employed in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are key structures in many drugs and functional materials. Its amine and boronic acid groups allow dual functionalization, making it valuable in the development of sensors, dyes, and conjugated materials. The boronic acid moiety enables specific binding to diols, such as in sugars and biomolecules, facilitating applications in biosensors, responsive drug delivery systems, and fluorescent probes for cellular imaging and tracking. Also applied in the synthesis of covalent organic frameworks (COFs) and as a reagent in bioconjugation for labeling biomolecules.

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inventory 5g
10-20 days ฿17,190.00

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(4-Aminophenyl)boronic acid hydrate
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals. Commonly employed in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are key structures in many drugs and functional materials. Its amine and boronic acid groups allow dual functionalization, making it valuable in the development of sensors, dyes, and conjugated materials. The boronic acid moiety enables specific binding to diols, such as in sugars and biomolecules, facilitating applications in bi

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals. Commonly employed in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are key structures in many drugs and functional materials. Its amine and boronic acid groups allow dual functionalization, making it valuable in the development of sensors, dyes, and conjugated materials. The boronic acid moiety enables specific binding to diols, such as in sugars and biomolecules, facilitating applications in biosensors, responsive drug delivery systems, and fluorescent probes for cellular imaging and tracking. Also applied in the synthesis of covalent organic frameworks (COFs) and as a reagent in bioconjugation for labeling biomolecules.

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