3-(Morpholin-2-yl)phenylboronic acid

95%

Reagent Code: #90002
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CAS Number 2225152-23-6

science Other reagents with same CAS 2225152-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.03406 g/mol
Formula C₁₀H₁₄BNO₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive compounds and materials science, where its structural properties contribute to the design of advanced polymers and catalysts. Its application extends to medicinal chemistry, where it aids in the synthesis of potential drug candidates targeting various diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿26,640.00
25mg
10-20 days ฿79,920.00
3-(Morpholin-2-yl)phenylboronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive compounds and materials science, where its structural properties contribute to the de

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive compounds and materials science, where its structural properties contribute to the design of advanced polymers and catalysts. Its application extends to medicinal chemistry, where it aids in the synthesis of potential drug candidates targeting various diseases.

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