3-Fluoro-5-(methylcarbamoyl)phenylboronic acid

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Reagent Code: #90172
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CAS Number 871332-63-7

science Other reagents with same CAS 871332-63-7

blur_circular Chemical Specifications

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Weight 196.97 g/mol
Formula C₈H₉BFNO₃
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MDL Number MFCD07363793
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is effective in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. Its structure, featuring a fluorine atom and a methylcarbamoyl group, enhances its reactivity and selectivity in these reactions, making it valuable for creating diverse chemical libraries. Additionally, it may be employed in the development of sensors or probes for detecting specific biological molecules, leveraging its ability to form stable complexes with diols and other functional groups.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿13,450.00

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3-Fluoro-5-(methylcarbamoyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is effective in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. Its structure, featuring a fluorine atom and a methylcarbamoyl group, enhances its reactivity and selectivity in these reactions, making it valuable for creating d

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is effective in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. Its structure, featuring a fluorine atom and a methylcarbamoyl group, enhances its reactivity and selectivity in these reactions, making it valuable for creating diverse chemical libraries. Additionally, it may be employed in the development of sensors or probes for detecting specific biological molecules, leveraging its ability to form stable complexes with diols and other functional groups.

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