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

98%

  • Product Code: 89620
  CAS:    1704068-63-2
Molecular Weight: 315.18 g./mol Molecular Formula: C₁₇H₂₂BNO₄
EC Number: MDL Number: MFCD22987683
Melting Point: Boiling Point:
Density: Storage Condition:  2-8°C
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.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.500 10-20 days $1,261.93
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2-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)isoindoline-1,3-dione
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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