2-fluoro-N-isopropyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
Reagent
Code: #90602
CAS Number
1689511-55-4
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Molecular Information
Weight
307.1681232 g/mol
Formula
C₁₆H₂₃BFNO₃
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Registry Numbers
MDL Number
MFCD31653840
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Storage & Handling
Storage
2-8°C, sealed, dry
description Product Description
This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The presence of the tetramethyl-1,3,2-dioxaborolane group makes it a valuable building block in Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds. Its application extends to the development of complex organic molecules, including those with potential therapeutic properties. Additionally, it is employed in the synthesis of boron-containing compounds, which are of interest in materials science and medicinal chemistry due to their unique properties and reactivity.
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2-fluoro-N-isopropyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The presence of the tetramethyl-1,3,2-dioxaborolane group makes it a valuable building block in Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds. Its application extends to the development of complex organic molecules, including those with potential therapeutic properties. Additionally, it is employed in the synthesis of boron-containing compounds, which are of interest in materials science and medicinal chemistry due to their unique properties and reactivity.
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