3-methyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide

95%

Reagent Code: #89976
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CAS Number 2246862-47-3

science Other reagents with same CAS 2246862-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.22046 g/mol
Formula C₂₀H₂₄BNO₃
badge Registry Numbers
MDL Number MFCD32206447
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for constructing complex molecules. Additionally, it is used in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and reactivity also make it suitable for research in material science, particularly in the development of organic electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,440.00
inventory 1g
10-20 days ฿50,544.00

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3-methyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide
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This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for constructing complex molecules. Additionally, it is used in the preparation of biologically active compounds, including potential drug candidates targ
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for constructing complex molecules. Additionally, it is used in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and reactivity also make it suitable for research in material science, particularly in the development of organic electronic materials.
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