2-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)isoindoline-1,3-dione

98%

Reagent Code: #89620
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CAS Number 1704068-63-2

science Other reagents with same CAS 1704068-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.18 g/mol
Formula C₁₇H₂₂BNO₄
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MDL Number MFCD22987683
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The presence of the tetramethyl dioxaborolane group makes it a stable and reactive boron source, enabling efficient coupling with aryl or vinyl halides. Additionally, its isoindoline-1,3-dione moiety can serve as a protecting group or be further modified to introduce functional groups into target molecules. Its applications extend to the development of advanced materials, such as polymers and ligands for catalysis, where precise control over molecular structure is essential.

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inventory 500mg
10-20 days ฿42,060.00

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2-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)isoindoline-1,3-dione
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This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The presence of the tetramethyl dioxaborolane group makes it a stable and reactive boron source, enabling efficient coupling with aryl or vinyl halides. Additionally, its

This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The presence of the tetramethyl dioxaborolane group makes it a stable and reactive boron source, enabling efficient coupling with aryl or vinyl halides. Additionally, its isoindoline-1,3-dione moiety can serve as a protecting group or be further modified to introduce functional groups into target molecules. Its applications extend to the development of advanced materials, such as polymers and ligands for catalysis, where precise control over molecular structure is essential.

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