3-Morpholinophenylboronic acid hydrochloride

≥98%

Reagent Code: #90126
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CAS Number 863248-20-8

science Other reagents with same CAS 863248-20-8

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scatter_plot Molecular Information
Weight 243.5 g/mol
Formula C₁₀H₁₄BNO₃HCl
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active molecules, aiding in drug discovery and medicinal chemistry research. Its boronic acid group makes it valuable in the design of sensors and probes for detecting specific analytes in biochemical studies. Additionally, it is utilized in the production of materials for organic electronics and advanced polymers.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,070.00
inventory 5g
10-20 days ฿7,560.00
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3-Morpholinophenylboronic acid hydrochloride
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Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active molecules, aiding in drug discovery and medicinal chemistry research. Its boronic acid group makes it valuable in the design of sensors and probes fo

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active molecules, aiding in drug discovery and medicinal chemistry research. Its boronic acid group makes it valuable in the design of sensors and probes for detecting specific analytes in biochemical studies. Additionally, it is utilized in the production of materials for organic electronics and advanced polymers.

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