3-Pyrrolidinylcarbonylphenylboronic acid

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Reagent Code: #90127
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CAS Number 723281-53-6

science Other reagents with same CAS 723281-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.05 g/mol
Formula C₁₁H₁₄BNO₃
badge Registry Numbers
MDL Number MFCD04115685
thermostat Physical Properties
Melting Point 113-116°C
Boiling Point 461.7°C
inventory_2 Storage & Handling
Density 1.26g/mL
Storage  2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive molecules and drug candidates due to its ability to introduce specific functional groups into complex structures. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,790.00
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3-Pyrrolidinylcarbonylphenylboronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive molecules and drug candidates due to its ability to introduce specific functional groups into complex

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive molecules and drug candidates due to its ability to introduce specific functional groups into complex structures. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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